Relevant bibliographies by topics / Allylic alcohols

Academic literature on the topic 'Allylic alcohols'

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Published: 4 June 2021
Last updated: 18 February 2022

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Journal articles on the topic "Allylic alcohols"

1

Ficeri, Vlastimír, Peter Kutschy, Milan Dzurilla, and Ján Imrich. "[3,3]- Versus [1,3]-Sigmatropic Rearrangement of O-Substituted Allyl N-Acylmonothiocarbamates." Collection of Czechoslovak Chemical Communications 59, no. 12 (1994): 2650–62. http://dx.doi.org/10.1135/cccc19942650.

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Substituted allylic alcohols (2-buten-1-ol, 1-buten-3-ol, cinnamyl alcohol and 3-methyl-2-buten-1-ol) react with acyl isothiocyanates (4-chlorobenzoyl, 2,6-difluorobenzoyl, 3-phenylpropenoyl, 2-thienocarbonyl, 3-chloro-2-thienocarbonyl and 3-chloro-2-benzo[b]thienocarbonyl isothiocyanate) with the formation of highly reactive O-substituted allyl N-acylmonothiocarbamates, which either spontaneously or by heating in boiling benzene undergo [3,3]-sigmatropic rearrangement to S-substituted allyl N-acylmonothiocarbamates. The structure of S-esters with isomerized allylic group affords the unequivocal evidence of the [3,3]-sigmatropic route of studied rearrangement. Further heating of [3,3]-rearranged N-(4-chlorobenzoyl)monothiocarbamates results in the [1,3]-sigmatropic shift of monothiocarbamate group. Using arylalkyl alcohols with the allylic double bond inserted into an aromatic system the obtained O-esters either do not undergo any rearrangement (benzyl alcohol) or undergo [1,3]-sigmatropic rearrangement (2- and 3-furylmethanol and 1-(2-furyl)ethanol) to the corresponding S-esters. For explanation of this reaction the tandem of [3,3]- and [1,3]-sigmatropic rearrangements is suggested.
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Wang, Jialiang, Wen Huang, Zhengxing Zhang, Xu Xiang, Ruiting Liu, and Xigeng Zhou. "FeCl3·6H2O Catalyzed Disproportionation of Allylic Alcohols and Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol." Journal of Organic Chemistry 74, no. 9 (May 2009): 3299–304. http://dx.doi.org/10.1021/jo900070q.

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Cooper, Matthew A., and A. David Ward. "Hydroxyselenation of allylic alcohols." Tetrahedron Letters 36, no. 13 (March 1995): 2327–30. http://dx.doi.org/10.1016/0040-4039(95)00247-a.

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Harada, Kohei, Marina Nogami, Keiichi Hirano, Daisuke Kurauchi, Hisano Kato, Kazunori Miyamoto, Tatsuo Saito, and Masanobu Uchiyama. "Allylic borylation of tertiary allylic alcohols: a divergent and straightforward access to allylic boronates." Organic Chemistry Frontiers 3, no. 5 (2016): 565–69. http://dx.doi.org/10.1039/c6qo00009f.

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Chern, Ching-Yuh, Ching-Chun Tseng, Rong-Hong Hsiao, Fung Fuh Wong, and Yueh-Hsiung Kuo. "Cyclopentadienyl Ruthenium(II) Complex-Mediated Oxidation of Benzylic and Allylic Alcohols to Corresponding Aldehydes." Heteroatom Chemistry 2019 (August 18, 2019): 1–8. http://dx.doi.org/10.1155/2019/5053702.

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This work reports an efficient method for the oxidation reaction of aliphatic, aromatic allylic, and benzylic alcohols into aldehydes catalyzed by the cyclopentadienyl ruthenium(II) complex (RuCpCl(PPh3)2) with bubbled O2. Through further optimizing controlled studies, the tendency order of oxidation reactivity was determined as follows: benzylic alcohols > aromatic allylic alcohols >> aliphatic alcohols. In addition, this method has several advantages, including a small amount of catalyst (0.5 mol%) and selective application of high discrimination activity of aliphatic, aromatic allylic, and benzylic alcohols.
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Akkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith, and Joseph S. M. Samec. "Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols." Synthesis 52, no. 05 (January 7, 2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.

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The Suzuki–Miyaura reaction is one of the most powerful tools for the formation of carbon–carbon bonds in organic synthesis. The utilization of alcohols in this powerful reaction is a challenging task. This short review covers progress in the transition-metal-catalyzed Suzuki­–Miyaura-type cross-coupling reaction of π-activated alcohol, such as aryl, benzylic, allylic, propargylic and allenic alcohols, between 2000 and June 2019.1 Introduction2 Suzuki–Miyaura Cross-Coupling Reactions of Aryl Alcohols2.1 One-Pot Reactions with Pre-activation of the C–O Bond2.1.1 Palladium Catalysis2.1.2 Nickel Catalysis2.2 Direct Activation of the C–O Bond2.2.1 Nickel Catalysis3 Suzuki–Miyaura-Type Cross-Coupling Reactions of Benzylic Alcohols4 Suzuki–Miyaura-Type Cross-Coupling Reactions of Allylic Alcohols4.1 Rhodium Catalysis4.2 Palladium Catalysis4.3 Nickel Catalysis4.4 Stereospecific Reactions4.5 Stereoselective Reactions4.6 Domino Reactions5 Suzuki–Miyaura-Type Cross-Coupling Reactions of Propargylic Alcohols5.1 Palladium Catalysis5.2 Rhodium Catalysis6 Suzuki–Miyaura-Type Cross-Coupling Reactions of Allenic Alcohols6.1 Palladium Catalysis6.2 Rhodium Catalysis7 Conclusions
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Hamada, Yoko, Rio Matsunaga, Tomoko Kawasaki-Takasuka, and Takashi Yamazaki. "Base-Mediated Claisen Rearrangement of CF3-Containing Bisallyl Ethers." Molecules 26, no. 14 (July 19, 2021): 4365. http://dx.doi.org/10.3390/molecules26144365.

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We have previously clarified that the strongly electron-withdrawing CF3 group nicely affected the base-mediated proton shift of CF3-containing propargylic or allylic alcohols to afford the corresponding α,β-unsaturated or saturated ketones, respectively, which was applied this time to the Claisen rearrangement after O-allylation of the allylic alcohols with a CF3 group, followed by isomerization to the corresponding allyl vinyl ethers via the proton shift, enabling the desired rearrangement in a tandem fashion, or in a stepwise manner, the latter of which was proved to have attained an excellent diastereoselectivity with the aid of a palladium catalyst.
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Jun, Chul-Ho, and Chang-Hee Lee. "Chelation-Assisted C–H and C–C Bond Activation of Allylic Alcohols by a Rh(I) Catalyst under Microwave Irradiation." Synlett 29, no. 06 (November 16, 2017): 736–41. http://dx.doi.org/10.1055/s-0036-1591697.

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Chelation-assisted Rh(I)-catalyzed ketone synthesis from allylic alcohols and alkenes through C–H and C–C bond activations under microwave irradiation was developed. Aldimine is formed via olefin isomerization of allyl alcohol under Rh(I) catalysis and condensation with 2-amino-3-picoline, followed by continuous C–H and C–C bond activations to produce a dialkyl ketone. The addition of piperidine accelerates the reaction rate by promoting aldimine formation under microwave conditions.
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Emayavaramban, Balakumar, Moumita Roy, and Basker Sundararaju. "Iron-Catalyzed Allylic Amination Directly from Allylic Alcohols." Chemistry - A European Journal 22, no. 12 (February 17, 2016): 3952–55. http://dx.doi.org/10.1002/chem.201505214.

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Berger, Anna Lucia, Karsten Donabauer, and Burkhard König. "Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones." Chemical Science 9, no. 36 (2018): 7230–35. http://dx.doi.org/10.1039/c8sc02038h.

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We report a photocatalytic version of the Barbier type reaction using readily available allyl or benzyl bromides and aromatic aldehydes or ketones as starting materials to generate allylic or benzylic alcohols.
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Dissertations / Theses on the topic "Allylic alcohols"

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Brennan, Meabh B. "Chemo- and stereoselective oxidation of allylic amino alcohols." Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531953.

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Hackett, Simon F. J. "Selective Oxidation of Allylic Alcohols on Palladium Catalysts." Thesis, University of York, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.490272.

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This thesis concerns the selective aerobic oxidation of allylic alcohols over practical and model palladium c~alysts. The goal was to elucidate the nature of the active catalyst site and origin of deactivation, which have hindered industrial implementation of such systems. It is hoped that understanding such fundamental aspects of the catalytic process will help optimise future· catalysts exhibiting high turnover frequencies as well as longer lifetimes on-stream. To realise these goals wet-chemical inorganic materials synthesis has been married with Ultra High Vacuum (UHV) single crystal methodologies. A series of amorphous, y-alumina supported palladium catalysts were prepared containing variable Pd concentrations. These allowed the impact of particle size on their resultant catalysis to be studied systematically. Characterising these small metal particles proved challenging, necessitating the combination of powerful bulk and surface sensitive techniques including X-ray Absorption (XAS) and Xray Photoelectron Spectroscopy (XPS) to identify the nature/structure ofthe active phase. These measurements revealed a progressive transformation from large metallic Pd clusters to small oxidised palladium clusters with decreasing precious metal loading. The concentration of surface palladium oxide correlated with the Turnover Frequency (TOF) towards the selective oxidation of both crotyl and cinnamyl alcohols. Surfactant templating routes were subsequently employed to produce high . surface, area mesoporous alumina supports, with a view to boosting the palladium dispersion and proportion of active metal oxide. Bulk and surface spectroscopies revealed similar trends in Pd cluster size and oxidation state with loading as observed for the amorphous supports, albeit with smaller more heavily oxidised palladium at the lowest loadings. High-resolution, high angle annular dark field (HAADF) scanning transmission electron microscopy (STEM) revealed that mesoporous alumina was able to stabilize isolated Pd(II) atoms on its surface. Synergy between these atomically-dispersed reduced palladium centers, and improved reactant/product mass transport through the mesoporous structure resulted in extremely active catalysts for alcohol selective oxidation. Decreasing II' II J _ _~ ~ t. ', ...... '... - - - ....:-. .• the Pd concentration increased TOFs as observed for the amorphous alumina catalysts. The single-site catalyst possessed initial TOFs of4400 and 7080 hr-I for cinnamyl and crotyl alcohol oxidation to their respective aldehydes. In order to shed insight into/the un~erlying reactant/surface interaction and deactivation mechanism, UHV studies were subsequently conducted over Pd(lll) single crystal surfaces, to model the most stable (111) facets of larger metal clusters found in practical oxidation catalysts. The adsorption geometry and thermal chemistry of both benzene and bromobenzene were first studied to examine the interaction of the phenyl group in cinnamyl alcohol with Pt(111). Fast XPS and NEXAFS spectra shoW that both benzene and bromobenzene adsorb non-dissociatively, but whilst the former bonds parallel to the surface, bromobenzene shows a significant tilt angle of-60°. Thermal-desorption spectroscopy showed that 20 % of a saturated benzene monolayer desorbs intact in two states, with the remainder undergoing successive dehydrogenations depositing surface-bound hydrocarbon fragments. For bromobenzene, low temperature C-Br bond cleavage results in surface-bound -phenyl groups. A proportion ofthese dehydrogenate at 400 K, liberating hydrogen which subsequently reacts with bromine, or other surface bound phenyls, yielding HBr, benzene and H2. Approximately 30% of a bromobenzene monolayer desorbs either reversibly or as reactively-formed hydrocarbons. The chemistry of crotyl alcohol was subsequently explored on clean and oxygen covered Pd (111) surfaces. Synchrotron X-ray experiments were 'combined with laboratory mass spectrometry to elucidate the associated binding geometry and reaction network. NEXAFS and Fast XPS revealed crotyl alcohol adsorbs molecularly at 95 K, with the allyl moiety parallel to the surface. Surface_ annealing induces oxidative dehydrogenation to crotonaldehyde at sub-ambient temperatures, in competition with a minor dehydration route to butene and water. Crucially, alcohol decarbonylation was also observed at catalytically relevant temperatures, resulting in an accumulation of surface bound CO and hydrocarbon fragments over the bare metal surface. Coadsorbed oxygen suppressed this decarbonylation pathway, promoting crotonaldehyde desorption over a similar temperature regime to that observed over dispersed PdfAh03 clusters.
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Gao, Y. (Yun). "Synthesis and synthetic transformations of allylic alcohols, epoxy alcohols, and 1,2-cyclic sulfates." Thesis, Massachusetts Institute of Technology, 1988. http://hdl.handle.net/1721.1/14588.

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Khan, Afzal. "Synthesis and reactions of epoxides." Thesis, University of Sheffield, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286509.

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Peters, Byron. "Iridium Catalysed Asymmetric Hydrogenation of Olefins and Isomerisation of Allylic Alcohols." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-122419.

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The work described in this thesis is focused on exploring the efficacy of asymmetric iridium catalysis in the hydrogenation of challenging substrates, including precursors to chiral sulfones and chiral cyclohexanes. Furthermore, iridium catalysis was used to isomerise allylic alcohols to aldehydes, and in a formal total synthesis of Aliskiren (a renin inhibitor). A large variety of unsaturated sulfones (cyclic, acyclic, vinylic, allylic and homoallylic) were prepared and screened in the iridium catalysed hydrogenation reaction using a series of previously developed N,P-ligated Ir-catalysts. The outcome was a highly enantioselective (>90% ee) protocol to prepare sulfones bearing chiral carbon scaffolds, sometimes having purely aliphatic substituents at the stereogenic centre. Furthermore, performing the Ramberg-Bäcklund reaction on the chiral products, under optimised conditions, produced cyclic and acyclic unsaturated derivatives without erosion of enantiomeric excess. This hydrogenation protocol was also successful in the hydrogenation of a number of cyclohexene-containing compounds. Minimally functionalised, functionalised and heterocycle-containing cyclohexenes were hydrogenated in up to 99% ee. Hitherto, both chiral sulfones and chiral cyclohexanes have been challenging targets for most catalytic asymmetric methodologies. Although the preparation of aldehydes and ketones by isomerisation of the corresponding allylic alcohol is well established, there has been limited success in the development of good enantioselective protocols. For the isomerisation of a number γ,γ-allylic alcohols to the corresponding chiral aldehydes, high enantioselectivities (up to >99% ee) and modest yields were achieved using an N,P-iridium catalyst. Noteworthy is the high selectivity obtained for isomerisation of Z and dialkyl γ,γ-allylic alcohols, which prior to this study had been difficult to isomerise in high enantioselectivity. Preparation of a key intermediate used in the synthesis of Aliskiren, a renin inhibitor drug was also accomplished. Using a convergent synthesis strategy, two allylic alcohol fragments were hydrogenated with high enantiomeric excess (>92% ee). These fragments were then joined using a Julia-Kocienski reaction, providing >95% E geometry around the C=C bond, which was crucial for the subsequent steps in the synthesis.

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 5: Manuscript.

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Smith, Torben J. N. "Enantioselective deprotonations of three membered rings." Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243768.

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Lee, Wai-Man. "Stereocontrolled synthesis of polysubstituted tetrahydropyrans and #delta#-lactones via tandem [2,3]-Wittig-anionic oxy-Cope rearrangement." Thesis, University of Liverpool, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243034.

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Evans, Paul. "The epoxy Ramberg Bäcklund rearrangement (ERBR) and related studies." Thesis, University of York, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265373.

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Otoo, Barnabas. "Conjugate Additions and Transposition of the Allylic Alcohols of Enol Ethers of 1, 2-Cyclohexanedione." Digital Commons @ East Tennessee State University, 2010. https://dc.etsu.edu/etd/1748.

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A variety of protected enolic forms of 1, 2-cyclohexanedione was prepared as substrates for conjugate addition studies using organocopper reagents. The sequence involved the enol ether preparation via the enolate, alkylation with an organometalic reagent, and oxidative rearrangement with pyridinium chlorochromate followed by the conjugate addition reactions. Protection of 1, 2-cyclohexanedione was achieved by reacting with chloro tert-butyldimethyl silane and subjected to alkylation. Steric problems were encountered and so an alternative protective group the methoxymethyl acetal was prepared and studied. Alkylation of these derivatives was successful; however, the oxidation was problematic and although evidence for rearrangement was observed in one case, it did not provide the desired ketone.
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Qiu, Shuai. "Trifluoromethoxylation of Allylic Alcohols via 1,2-Aryl Migration Promoted by Visible Light-Mediated Photoredox Catalysis." Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278836.

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Visible light photoredox catalysis has proven to be a powerful tool for promoting transformations in organic synthesis. Hence this project was carried out to develop tools for predicting reactivity patterns of visible light- promoted redox reactions. Fluorination is of immense importance in organic chemistry, and so is trifluoromethoxylation. The fluorination reaction has been studied for a long time and has been accomplished in milder ways, while the generation of a trifluoromethoxy-radical at room temperature and atmospheric pressure remains a challenge. The design of the reaction in this project is to overcome the instability and take control of the catalytic event under visible- light photocatalytic conditions. The trifluoromethoxylation reaction proceeded at room temperature with the reaction time of 60 min using acetonitrile as the solvent and blue LED (10 W) as the external light source. No yield of the desired product was obtained for any of the substrates. More surprisingly, in all entries, 3,3-diphenylprop-2-en-1-ol was attained as a side product. The same side product was also detected in the entry with ambient light, concluding that the reaction was completed without any external light source. Thus, no photoredox catalysis took place.
Fotoredoxkatalys via ljus inom det synliga spektrat har visat sig vara ett kraftfullt verktyg för att gynna reaktioner inom organisk syntes. Detta projekt genomfördes med syfte att utveckla verktyg avsedda för att förutspå reaktivitetsmönster vid fotoredoxkatalys med synligt ljus. Fluorinering och trifluorometoxylering är viktiga verktyg inom organisk syntes. Fluorineringsreaktionen har studerats länge och har kunnat genomföras under milda reaktionsbetingelser, medan generering av trifluorometoxyradikal vid rumstemperatur och atomsfärstryck fortfarande är en utmaning. Reaktionen i det här projektet är designad för att kringgå instabilitetsproblemet och ta kontroll över katalysmomentet, under fotokatalysförhållanden i synligt ljus. Reaktionen utfördes i rumstemperatur med en reaktionstid på 60 minuter, med acetonitril som lösningsmedel och blå LED (10 W) som extern ljuskälla. Inget av substraten reagerade till den önskade produkten. Mer överraskande var att 3,3-difenylprop-2-en-1-ol erhölls som sidoprodukt vid alla reaktionsstillfällen. Samma sidoprodukt upptäcktes även vid reaktion genomförd i dagsljus, vilket indikerar att reaktionen skedde utan någon extern ljuskälla. Således skedde ingen fotoredoxkatalys.
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Books on the topic "Allylic alcohols"

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Loutchnikov, Andrei. Rhodium-catalyzed coupling reactions of multisubstituted alkenes, arylsubstituted allylic amines, esters and alcohols with arylboronic acids in aqueous media. Ottawa: National Library of Canada, 2003.

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Ariru arukōru: Allyl alcohol. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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Courtin, Helene L. Oxidation of allyl alcohol into glycerol by hydrogen peroxideoverTI-ZSM-5. Manchester: UMIST, 1994.

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Loutchinkov, Andrei. Rhodium-catalyzed coupling reactions of multisubstituted alkenes, arylsubstituted allylic amines, esters and alcohols with arylboronic acids in aqueous media. 2003, 2003.

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Book chapters on the topic "Allylic alcohols"

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Surh, Young-Joon. "Sulfotransferase-Mediated Activation of Some Benzylic and Allylic Alcohols." In Advances in Experimental Medicine and Biology, 339–45. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4757-9480-9_41.

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Johnson, Roy A., and K. Barry Sharpless. "Asymmetric Oxidations and Related Reactions: Catalytic Asymmetric Epoxidation of Allylic Alcohols." In Catalytic Asymmetric Synthesis, 229–80. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721506.ch7.

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Fu, Ming-Chen. "Efficient Pd-Catalyzed Regio- and Stereoselective Carboxylation of Allylic Alcohols with Formic Acid." In Springer Theses, 77–105. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-7623-2_4.

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Hodgson, D. M., and P. G. Humphreys. "Allylic Substitution." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00495.

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Hodgson, D. M., and P. G. Humphreys. "Allylic Rearrangements." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00549.

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Eames, J. "Isomerization of Allylic Alcohols." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00341.

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Eames, J. "Hydroxylation of Allylic Alcohols." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00346.

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Eames, J. "Dihydroxylation of Allylic Alcohols." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00348.

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Eames, J. "Epoxidation of Allylic Alcohols." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00349.

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Eames, J. "Cyclopropanation of Allylic Alcohols." In Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00353.

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Conference papers on the topic "Allylic alcohols"

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HENRIQUE FREIRE ARAUJO, LUIZ, José Augusto Rosário Rodrigues, FABIO NASARIO, and Paulo José Samenho Moran. "Biocatalytic Redox Reactions with Allylic Alcohols." In XXV Congresso de Iniciação Cientifica da Unicamp. Campinas - SP, Brazil: Galoa, 2017. http://dx.doi.org/10.19146/pibic-2017-78725.

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Lattanzi, Alessandra, Antonio Proto, and Arrigo Scettri. "Titanocenes Catalyzed Diastereoselective Epoxidation of Allylic Alcohols." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01747.

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Tabarelli, Greice, Marcelo Godoi, Fábio Z. Galetto, and Antonio Luiz Braga. "Microwave-assisted solvent- and catalyst-free synthesis of allylic thioetheres from allylic alcohols." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0127-1.

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Rosário Rodrigues, José Augusto, and NatÁlia Maria Polidoro. "Cascade Redox Reactions with allylic alcohols in biocatalysis." In XXIII Congresso de Iniciação Científica da Unicamp. Campinas - SP, Brazil: Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-37703.

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Maria Polidoro, NatÁlia, José Augusto Rosário Rodrigues, FABIO NASARIO, and Paulo José Samenho Moran. "Biocatalytic redox reactions of allylic alcohols catalysed by microorgansims." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Campinas - SP, Brazil: Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-51178.

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Oliveira, Caio C., and Carlos Roque D. Correia. "Studies on the Regio- and Enantioselective Heck Arylations of Acyclic Allylic Alcohols." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013913141742.

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Matyushov, V. F., A. L. Tolstov, L. V. Kobryna, P. S. Yaremov, V. G. Ilyin, and E. V. Lebedev. "Facile synthesis of catalytically active porous titanosilicates for liquid-phase epoxidation of allyl alcohol with hydrogen peroxide." In 2016 International Conference on Nanomaterials: Application & Properties (NAP). IEEE, 2016. http://dx.doi.org/10.1109/nap.2016.7757262.

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