Einloggen

Thematische Bibliographien / Isochromans / Zeitschriftenartikel

Zeitschriftenartikel zum Thema „Isochromans“

Um die anderen Arten von Veröffentlichungen zu diesem Thema anzuzeigen, folgen Sie diesem Link: Isochromans.

Autor: Grafiati

Veröffentlicht am 20. Juli 2024

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit Top-50 Zeitschriftenartikel für die Forschung zum Thema "Isochromans" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Sehen Sie die Zeitschriftenartikel für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.

1

Hamada, Shohei, Kyoko Yano, Ayano Ohshimo, Elghareeb E. Elboray, Yusuke Kobayashi und Takumi Furuta. „Oxidative C–N Bond Formation of Isochromans Using an Electronically Tuned Nitroxyl Radical as Catalyst“. SynOpen 08, Nr. 02 (Mai 2024): 125–29. http://dx.doi.org/10.1055/s-0040-1720118.

Der volle Inhalt der Quelle

Annotation:

AbstractThe cross-dehydrogenative coupling between isochromans and nucleophiles using an electronically tuned nitroxyl radical catalyst, which effectively promotes the oxidation of benzylic ethers, has been investigated. Using sulfonamides as a nucleophile, modification of isochromans via oxidative C–N bond formation has been achieved at ambient temperature.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

Liu, Shiyao, Kazunari Nakajima und Yoshiaki Nishibayashi. „Copper-catalysed enantioselective intramolecular etherification of propargylic esters: synthetic approach to chiral isochromans“. RSC Advances 9, Nr. 33 (2019): 18918–22. http://dx.doi.org/10.1039/c9ra03880a.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

Trefiletti, Giuliana, Anna Rita Togna, Valentina Latina, Carolina Marra, Marcella Guiso und Giuseppina I. Togna. „1-Phenyl-6,7-dihydroxy-isochroman suppresses lipopolysaccharide-induced pro-inflammatory mediator production in human monocytes“. British Journal of Nutrition 106, Nr. 1 (27.01.2011): 33–36. http://dx.doi.org/10.1017/s0007114510005763.

Der volle Inhalt der Quelle

Annotation:

Extra-virgin olive oil is an integral ingredient of the Mediterranean diet, and it has been suggested that its high consumption has beneficial effects on human health. Its protective effect, in particular against the development of CVD, has been related not only to the high content of oleic acid, but also to the antioxidant and anti-inflammatory properties of polyphenols. In order to verify the anti-inflammatory and anti-atherogenic properties of hydroxy-isochromans, a class of ortho-diphenols present in extra-virgin olive oil, we investigated the potential ability of 1-phenyl-6,7-dihydroxy-isochroman (L137) to modulate the production of key inflammatory mediators by human monocytes, by evaluating its in vitro effects on prostanoid (thromboxane A2 and PGE2) and cytokine (TNF-α) production. Its effect on the protein expression of the inducible form of cyclo-oxygenase-2 (COX-2), a pro-inflammatory enzyme responsible for elevated prostanoid levels, was also explored. The results showed that L137 significantly inhibited both prostanoid and TNF-α production in lipopolysaccharide-primed human monocytes in a dose-dependent manner, by inhibiting the COX activity of COX-2. We also demonstrated that the effects of the isochroman are mediated, at least partly, through the suppression of NF-κB activation leading to the down-regulation of the synthesis of COX-2.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

UNTERHALT, B., und R. JOESTINGMEIER. „ChemInform Abstract: New Substituted Isochromans.“ ChemInform 28, Nr. 1 (04.08.2010): no. http://dx.doi.org/10.1002/chin.199701169.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

Verma, Ashish Kumar, Ande Chennaiah, Sateesh Dubbu und Yashwant D. Vankar. „Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet–Spengler reaction“. Organic & Biomolecular Chemistry 16, Nr. 37 (2018): 8258–62. http://dx.doi.org/10.1039/c8ob01698d.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

Thatikonda, Thanusha, Siddharth K. Deepake, Pawan Kumar und Utpal Das. „α-Angelica lactone catalyzed oxidation of benzylic sp3 C–H bonds of isochromans and phthalans“. Organic & Biomolecular Chemistry 18, Nr. 21 (2020): 4046–50. http://dx.doi.org/10.1039/d0ob00729c.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

Nickerson, Leslie A., Benjamin D. Bergstrom, Mingchun Gao, Yuan-Shin Shiue, Croix J. Laconsay, Matthew R. Culberson, Walker A. Knauss, James C. Fettinger, Dean J. Tantillo und Jared T. Shaw. „Correction: Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C–H insertion of donor/donor carbenes“. Chemical Science 11, Nr. 19 (2020): 5113. http://dx.doi.org/10.1039/d0sc90081h.

Der volle Inhalt der Quelle

Annotation:

Correction for ‘Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C–H insertion of donor/donor carbenes’ by Leslie A. Nickerson et al., Chem. Sci., 2020, 11, 494–498, DOI: 10.1039/C9SC05111B.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

8

Unterhalt, B., und U. Heppert. „ChemInform Abstract: Isochromans Related to Fluoxetin.“ ChemInform 32, Nr. 38 (24.05.2010): no. http://dx.doi.org/10.1002/chin.200138108.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

9

Zhu, Zhengbo, Alafate Adili, Chenfei Zhao und Daniel Seidel. „Catalytic Enantioselective Approaches to the oxa-Pictet–Spengler Cyclization and Other 3,6-Dihydropyran-Forming Reactions“. SynOpen 03, Nr. 03 (Juli 2019): 77–90. http://dx.doi.org/10.1055/s-0039-1690686.

Der volle Inhalt der Quelle

Annotation:

This Short Review provides an analysis of the state-of-the-art in catalytic enantioselective oxa-Pictet–Spengler cyclizations. Also discussed are other catalytic reactions providing access to enantioenriched isochromans and tetrahydropyrano[3,4-b]indoles. Context is provided and remaining challenges are highlighted.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

10

Yang, Guoping, Ke Li, Kai Zeng, Yijin Li, Tao Yu und Yufeng Liu. „Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate“. RSC Advances 11, Nr. 18 (2021): 10610–14. http://dx.doi.org/10.1039/d1ra01004b.

Der volle Inhalt der Quelle

Annotation:

An efficient heterogeneous and green catalyst [HEMTH]H₂[PMo₁₂O₄₀] was prepared to catalysis the oxa-Pictet–Spengler cyclization of arylethanols and aldehydes to afford isochromans with excellent yields using dimethyl carbonate as a green solvent.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

11

Huo, Congde, Mingxia Wu, Fengjuan Chen, Xiaodong Jia, Yong Yuan und Haisheng Xie. „Catalytic amounts of CBr4 mediated dehydrogenative coupling of isochromans with aromatic ketones“. Chemical Communications 51, Nr. 22 (2015): 4708–11. http://dx.doi.org/10.1039/c4cc09922b.

Der volle Inhalt der Quelle

Annotation:

In the presence of catalytic amounts of CBr₄ (a metal-free mediator), an unexpected oxidative dehydrogenative coupling of isochromans with ketones occurred to construct new C^sp3–C^sp3 bonds. The reactions were performed under simple solvent-free aerobic conditions.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

12

Ahmar, M., und R. Bloch. „A New Synthesis of Isochromans and Phtalans“. Synthetic Communications 22, Nr. 10 (Mai 1992): 1417–20. http://dx.doi.org/10.1080/00397919208021607.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

13

McMullin, David R., Tienabe K. Nsiama und J. David Miller. „Isochromans and α-Pyrones from Penicillium corylophilum“. Journal of Natural Products 77, Nr. 2 (23.01.2014): 206–12. http://dx.doi.org/10.1021/np4005486.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

14

Guiso, Marcella, Carolina Marra und Claudia Cavarischia. „Isochromans from 2-(3′,4′-dihydroxy)phenylethanol“. Tetrahedron Letters 42, Nr. 37 (September 2001): 6531–34. http://dx.doi.org/10.1016/s0040-4039(01)01307-7.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

15

Togna, Giuseppina I., Anna Rita Togna, Matteo Franconi, Carolina Marra und Marcella Guiso. „Olive Oil Isochromans Inhibit Human Platelet Reactivity“. Journal of Nutrition 133, Nr. 8 (01.08.2003): 2532–36. http://dx.doi.org/10.1093/jn/133.8.2532.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

16

Vankar, Yashwant, Parasuraman Rajasekaran und Yakkala Mallikharjunarao. „Synthesis of 1C-Aryl/Alkyl 2C-Branched Sugar-Fused Isochroman Derivatives by Sequential Prins and Friedel–Crafts Cyclizations on a Perlin Aldehyde Derived Substrate“. Synlett 28, Nr. 11 (09.03.2017): 1346–52. http://dx.doi.org/10.1055/s-0036-1588156.

Der volle Inhalt der Quelle

Annotation:

The synthesis of C-aryl/alkyl 2C-branched sugar-fused isochromans by using a carbohydrate-derived starting material is described. Our approach makes use of sequential Prins and Friedel–Crafts cyclizations in which a Perlin aldehyde derived homoallylic alcohol is converted into the target molecule. This strategy works well with many aldehydes and gives good yields with excellent selectivity.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

17

Khilya, V., O. Shablykina, M. Tsapko, S. Shilin, V. Moskvina, H. Bubela und Yu Zabolotna. „Eu(fod)3 EFFECT ON 1H NMR SPECTRA OF 3-ARYLISOCOUMARINS AND 3-ARYL-3,4-DIHYDROISOCOUMARINS WITH ALKOXY, ESTER AND AMIDE GROUPS“. Bulletin of Taras Shevchenko National University of Kyiv. Chemistry, Nr. 2(54) (2017): 74–80. http://dx.doi.org/10.17721/1728-2209.2017.2(54).15.

Der volle Inhalt der Quelle

Annotation:

The effect of the lanthanide shift reagent (LSR) – tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octa-dionate) of Europium – Eu(fod)3 – on 1H NMR spectra of functionalized 3-arylisocoumarins and 3-aryl-3,4-dihydroisocoumarins was investigated. Based on previous studies of LSR interactions with benzopyrones, it was expected that the main coordination centre for the Eu3+ would be the exocyclic Oxygen atom of the heterocycle, but the possibility of competition from aromatic substituent functional groups was also considered. By measuring lanthanide-induced shifts (LIS) of the proton signals of the molecules at different ratios of substrate and Eu(fod)3, specific LIS values were determined. Based on those, it was concluded that the main direction of LSR coordination with 3-(2-hydroxy-5-methylphenyl)-1Hisochromen-1-one, 3-(2-methoxy-5-methylphenyl)-1H-isochromen-1-one and 3-(2-methoxy-5-methylphenyl)isochroman-1-one is the exocyclic Oxygen atom of the heterocycle, because the maximum LIS were recorded for the H-8 atom of isochromone system of these derivatives. In the case of ethyl ester of [2-(4-(1-oxo-1H-isochromen-3-yl)phenoxy] acetic acid and methyl ester of [2-(4-(1-oxoisochroman-3-yl)phenoxy]acetic acid comparable LIS values were observed both for H-8 and for the methylene group of the hydroxyacetic acid fragment, therefore, in such molecules the coordination of the Eu3+ to the heterocycle or to the aliphatic ester group is almost equally probable. In spectrum of methyl ester of N-{[4-(1-oxo-1H-isochromen-3-yl)phenoxy]acetyl}valine and N-{[4-(1-oxoisochroman-3-yl)-phenoxy]acetyl}valine there are insignificant LIS of H-8; and the maximum LIS were observed for the signals of the protons neighboring the two carbonyl groups of hydroxyacetic acid and valine fragments. Thus, these compounds interact w

APA, Harvard, Vancouver, ISO und andere Zitierweisen

18

Yus, Miguel, Francisco Foubelo und Daniel García. „Cyclic Acetals as Precursors of Substituted Isochromans and Naphthoxepines“. HETEROCYCLES 74, Nr. 1 (2007): 507. http://dx.doi.org/10.3987/com-07-s(w)29.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

19

Mao, Ying, Min Cao, Xiaoguang Pan, Jiancheng Huang, Jing Li, Liren Xu und Lei Liu. „Bimolecular oxidative C–H alkynylation of α-substituted isochromans“. Organic Chemistry Frontiers 6, Nr. 12 (2019): 2028–31. http://dx.doi.org/10.1039/c9qo00352e.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

20

Zhou, Mei-Yan, Shan-Shan Kong, Ling-Qiong Zhang, Ming Zhao, Jin-Ao Duan, Zhen Ou-yang und Min Wang. „CuBr2 catalyzed bromination/oxidation of isochromans to benzaldehyde derivatives“. Tetrahedron Letters 54, Nr. 30 (Juli 2013): 3962–64. http://dx.doi.org/10.1016/j.tetlet.2013.05.078.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

21

AHMAR, M., und R. BLOCH. „ChemInform Abstract: A New Synthesis of Isochromans and Phthalans.“ ChemInform 23, Nr. 38 (21.08.2010): no. http://dx.doi.org/10.1002/chin.199238161.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

22

Leibeling, Markus, Dennis C. Koester, Martin Pawliczek, Svenia C. Schild und Daniel B. Werz. „Domino access to highly substituted chromans and isochromans from carbohydrates“. Nature Chemical Biology 6, Nr. 3 (24.01.2010): 199–201. http://dx.doi.org/10.1038/nchembio.302.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

23

Dammacco, Mariangela, Leonardo Degennaro, Saverio Florio, Renzo Luisi, Biagia Musio und Angela Altomare. „Lithiation ofN-Alkyl-(o-tolyl)aziridine: Stereoselective Synthesis of Isochromans§“. Journal of Organic Chemistry 74, Nr. 16 (21.08.2009): 6319–22. http://dx.doi.org/10.1021/jo9011943.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

24

Guiso, Marcella, Carolina Marra und Rocio Rodriguez Arcos. „An investigation on dihydroxy-isochromans in extra virgin olive oil“. Natural Product Research 22, Nr. 16 (10.11.2008): 1403–9. http://dx.doi.org/10.1080/14786410701823942.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

25

Zhou, Mei-Yan, Shan-Shan Kong, Ling-Qiong Zhang, Ming Zhao, Jin-Ao Duan, Ou-yang Zhen und Min Wang. „ChemInform Abstract: CuBr2Catalyzed Bromination/Oxidation of Isochromans to Benzaldehyde Derivatives.“ ChemInform 44, Nr. 44 (14.10.2013): no. http://dx.doi.org/10.1002/chin.201344065.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

26

Chen, Yan, und Shi-Kai Tian. „Decarboxylative Alkylation ofβ-Keto Acids with Isochromans under Oxidative Conditions“. Chinese Journal of Chemistry 31, Nr. 1 (27.12.2012): 37–39. http://dx.doi.org/10.1002/cjoc.201200994.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

27

Alavala, Gopi Krishna Reddy, Farrukh Sajjad, Taoda Shi, Zhenghui Kang, Mingliang Ma, Dong Xing und Wenhao Hu. „Diastereoselective synthesis of isochromans via the Cu(ii)-catalysed intramolecular Michael-type trapping of oxonium ylides“. Chemical Communications 54, Nr. 89 (2018): 12650–53. http://dx.doi.org/10.1039/c8cc06390g.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

28

Wei, Xiaoyi, Liangxiong Xu, Jinghua Xue, Hanhong Xu, Xingzhong Liu und Wenzhe Ma. „Three New Isochromans from the Mycelial Culture of a Cylindrocarpon Fungus“. HETEROCYCLES 68, Nr. 9 (2006): 1955. http://dx.doi.org/10.3987/com-06-10799.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

29

Petrone, David A., Hasnain A. Malik, Antonin Clemenceau und Mark Lautens. „Functionalized Chromans and Isochromans via a Diastereoselective Pd(0)-Catalyzed Carboiodination“. Organic Letters 14, Nr. 18 (06.09.2012): 4806–9. http://dx.doi.org/10.1021/ol302111y.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

30

Wang, Zhong, Peng Fan, Tong-Dan Xue, Lin-Lin Meng, Wen-Bin Gao, Jun Zhang, You-xing Zhao und Du-Qiang Luo. „Two New Isocoumarin Derivatives from an Endophytic Fungi Pestalotiopsis coffeae Isolated from a Mangrove Fishtail Palm“. Natural Product Communications 13, Nr. 1 (Januar 2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300117.

Der volle Inhalt der Quelle

Annotation:

Two new isocoumarin derivatives, 6,8-dihydroxy-7-methyl-1-oxo-1H-isochromene-3-carboxylic acid (1) and 6,8-dihydroxy-3-methoxy-3,7- dimethyl-isochroman-1-one (2), together with five known compounds (3-7), were isolated from the endophytic fungus Pestalotiopsis coffeae derived from the Chinese plant fishtail palm. The structures of these compounds were determined mainly by analysis of their NMR spectroscopic data. The structure of compound 2 was further confirmed by X-ray diffraction.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

31

Ammann, Stephen E., Grant T. Rice und M. Christina White. „Terminal Olefins to Chromans, Isochromans, and Pyrans via Allylic C–H Oxidation“. Journal of the American Chemical Society 136, Nr. 31 (16.07.2014): 10834–37. http://dx.doi.org/10.1021/ja503322e.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

32

Hegedüs, Adrienn, und Zoltán Hell. „Zeolite-catalyzed simple synthesis of isochromans via the oxa-Pictet–Spengler reaction“. Organic & Biomolecular Chemistry 4, Nr. 7 (2006): 1220. http://dx.doi.org/10.1039/b601314g.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

33

Zhou, Jimei, Chao Wang, Dong Xue, Weijun Tang, Jianliang Xiao und Chaoqun Li. „Synthesis of isochromans via Fe(OTf)2-catalyzed Oxa-Pictet–Spengler cyclization“. Tetrahedron 74, Nr. 49 (Dezember 2018): 7040–46. http://dx.doi.org/10.1016/j.tet.2018.10.028.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

34

Temperini, Andrea, Anna Barattucci, Paola Maria Bonaccorsi, Ornelio Rosati und Lucio Minuti. „Stereoselective Synthesis of Substituted Tetrahydropyrans and Isochromans by Cyclization of Phenylseleno Alcohols“. Journal of Organic Chemistry 80, Nr. 16 (11.08.2015): 8102–12. http://dx.doi.org/10.1021/acs.joc.5b01199.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

35

Liu, Jian, Elizabeth T. Birzin, Wanda Chan, Yi Tien Yang, Lee-Yuh Pai, Carolyn DaSilva, Edward C. Hayes et al. „Estrogen receptor ligands. Part 11: Synthesis and activity of isochromans and isothiochromans“. Bioorganic & Medicinal Chemistry Letters 15, Nr. 3 (Februar 2005): 715–18. http://dx.doi.org/10.1016/j.bmcl.2004.11.018.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

36

Cui, Jian-Fang, Bin Yang, Qiong Yu, Nathanael Chun-Him Lai, Han Chen und Man-Kin Wong. „Silver-Mediated Organic Transformations of Propargylamines to Enones, α-Thioketones, and Isochromans“. ChemistrySelect 4, Nr. 4 (29.01.2019): 1476–82. http://dx.doi.org/10.1002/slct.201900024.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

37

Leibeling, Markus, Bastian Milde, Daniel Kratzert, Dietmar Stalke und Daniel B. Werz. „Intermolecular Twofold Carbopalladation/Cyclization Sequence to Access Chromans and Isochromans from Carbohydrates“. Chemistry - A European Journal 17, Nr. 36 (02.08.2011): 9888–92. http://dx.doi.org/10.1002/chem.201101917.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

38

Kock, Ines, Siegfried Draeger, Barbara Schulz, Brigitta Elsässer, Tibor Kurtán, Ágnes Kenéz, Sándor Antus et al. „Pseudoanguillosporin A and B: Two New Isochromans Isolated from the Endophytic FungusPseudoanguillosporasp.“ European Journal of Organic Chemistry 2009, Nr. 9 (März 2009): 1427–34. http://dx.doi.org/10.1002/ejoc.200801083.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

39

Zeh, Michael, Peter Lorenz, Peter Kreutzmann und Peter Schönfeld. „Hydroxy-1-aryl-isochromans: protective compounds against lipid peroxidation and cellular nitrosative stress“. Redox Report 13, Nr. 1 (Februar 2008): 23–30. http://dx.doi.org/10.1179/135100008x259123.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

40

Kaufman, Teodoro S., und Enrique L. Larghi. „The Oxa-Pictet-Spengler Cyclization: Synthesis of Isochromans and Related Pyran-Type Heterocycles“. Synthesis, Nr. 2 (2006): 187–220. http://dx.doi.org/10.1055/s-2005-918502.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

41

Bovicelli, Paolo, Anna Sanetti, Roberta Bernini und Paolo Lupattelli. „Oxyfunctionalisation of activated methylenes by dimethyldioxirane: An easy conversion of isochromans into isocoumarins“. Tetrahedron 53, Nr. 28 (Juli 1997): 9755–60. http://dx.doi.org/10.1016/s0040-4020(97)00622-4.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

42

Xu, Yao-Chang, Elaine Lebeau, John W. Gillard und Giorgio Attardo. „Regio- and stereoselective DDQ-induced oxidative coupling of isochromans and isothiochroman with alcohols“. Tetrahedron Letters 34, Nr. 24 (Juni 1993): 3841–44. http://dx.doi.org/10.1016/s0040-4039(00)79242-2.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

43

Obata, Tomoyuki, Sho Suzuki, Asuka Nakagawa, Ryota Kajihara, Keiichi Noguchi und Akio Saito. „Gold-Catalyzed Domino Synthesis of Functionalized Benzofurans and Tetracyclic Isochromans via Formal Carboalkoxylation“. Organic Letters 18, Nr. 16 (02.08.2016): 4136–39. http://dx.doi.org/10.1021/acs.orglett.6b02159.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

44

Hashida, Junko, Megumi Niitsuma, Masato Iwatsuki, Mihoko Mori, Aki Ishiyama, Miyuki Namatame, Aki Nishihara-Tsukashima et al. „Panowamycins A and B, new antitrypanosomal isochromans produced by Streptomyces sp. K07-0010“. Journal of Antibiotics 65, Nr. 4 (25.01.2012): 197–202. http://dx.doi.org/10.1038/ja.2011.139.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

45

Huo, Congde, Mingxia Wu, Fengjuan Chen, Xiaodong Jia, Yong Yuan und Haisheng Xie. „ChemInform Abstract: Catalytic Amounts of CBr4Mediated Dehydrogenative Coupling of Isochromans with Aromatic Ketones.“ ChemInform 46, Nr. 29 (Juli 2015): no. http://dx.doi.org/10.1002/chin.201529194.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

46

Chen, Yan, und Shi-Kai Tian. „ChemInform Abstract: Decarboxylative Alkylation of β-Keto Acids with Isochromans under Oxidative Conditions.“ ChemInform 44, Nr. 43 (07.10.2013): no. http://dx.doi.org/10.1002/chin.201343139.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

47

Petrone, David A., Hasnain A. Malik, Antonin Clemenceau und Mark Lautens. „ChemInform Abstract: Functionalized Chromans and Isochromans via a Diastereoselective Pd(0)-Catalyzed Carboiodination.“ ChemInform 44, Nr. 3 (15.01.2013): no. http://dx.doi.org/10.1002/chin.201303126.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

48

Syed Abuthahir, S., M. NizamMohideen, S. Mayakrishnan, N. Uma Maheswari und V. Viswanathan. „Crystal structures of two new isocoumarin derivatives: 8-amino-6-methyl-3,4-diphenyl-1H-isochromen-1-one and 8-amino-3,4-diethyl-6-methyl-1H-isochromen-1-one“. Acta Crystallographica Section E Crystallographic Communications 75, Nr. 8 (09.07.2019): 1117–22. http://dx.doi.org/10.1107/s2056989019009435.

Der volle Inhalt der Quelle

Annotation:

The title compounds, 8-amino-6-methyl-3,4-diphenyl-1H-isochromen-1-one, C22H17NO2, (I), and 8-amino-3,4-diethyl-6-methyl-1H-isochromen-1-one, C14H17NO2, (II), are new isocoumarin derivatives in which the isochromene ring systems are planar. Compound II crystallizes with two independent molecules (A and B) in the asymmetric unit. In I, the two phenyl rings are inclined to each other by 56.41 (7)° and to the mean plane of the 1H-isochromene ring system by 67.64 (6) and 44.92 (6)°. In both compounds, there is an intramolecular N—H...O hydrogen bond present forming an S(6) ring motif. In the crystal of I, molecules are linked by N—H...π interactions, forming chains along the b-axis direction. A C—H...π interaction links the chains to form layers parallel to (100). The layers are then linked by a second C—H...π interaction, forming a three-dimensional structure. In the crystal of II, the two independent molecules (A and B) are linked by N—H...O hydrogen bonds, forming –A–B–A–B– chains along the [101] direction. The chains are linked into ribbons by C—H...π interactions involving inversion-related A molecules. The latter are linked by offset π–π interactions [intercentroid distances vary from 3.506 (1) to 3.870 (2) Å], forming a three-dimensional structure.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

49

Bianco, A., F. Coccioli, M. Guiso und C. Marra. „The occurrence in olive oil of a new class of phenolic compounds: hydroxy-isochromans“. Food Chemistry 77, Nr. 4 (Juni 2002): 405–11. http://dx.doi.org/10.1016/s0308-8146(01)00366-1.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

50

Mohler, Debra L., und David W. Thompson. „Synthesis of isochromans via the titanium tetrachloride assisted cyclization of acetals of phenethyl alcohols“. Tetrahedron Letters 28, Nr. 23 (Januar 1987): 2567–70. http://dx.doi.org/10.1016/s0040-4039(00)96149-5.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!