Добірка наукової літератури з теми "Spirocyclic molecules"
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Статті в журналах з теми "Spirocyclic molecules"
Fominova, Kateryna, Taras Diachuk, Dmitry Granat, Taras Savchuk, Vladyslav Vilchynskyi, Oleksiy Svitlychnyi, Vladyslav Meliantsev, et al. "Oxa-spirocycles: synthesis, properties and applications." Chemical Science 12, no. 34 (2021): 11294–305. http://dx.doi.org/10.1039/d1sc03615g.
Повний текст джерелаBenabdallah, Mohammed, Oualid Talhi, Fatiha Nouali, Nouredine Choukchou-Braham, Khaldoun Bachari, and Artur M. S. Silva. "Advances in Spirocyclic Hybrids: Chemistry and Medicinal Actions." Current Medicinal Chemistry 25, no. 31 (October 16, 2018): 3748–67. http://dx.doi.org/10.2174/0929867325666180309124821.
Повний текст джерелаPaquette, Leo A. "Spirocyclic Restriction of Nucleosides." Australian Journal of Chemistry 57, no. 1 (2004): 7. http://dx.doi.org/10.1071/ch03267.
Повний текст джерелаShen, Guo-Liang, Jing Sun, and Chao-Guo Yan. "Construction of dispirocyclohexyl-3,3′-bisoxindole and dispirocyclopentyl-3,3′-bisoxindole via domino cycloaddition reactions of N-benzylbenzimidazolium salts with 2-(2-oxoindolin-3-ylidene)acetates." RSC Advances 5, no. 6 (2015): 4475–83. http://dx.doi.org/10.1039/c4ra13760d.
Повний текст джерелаKappen, Lizzy S., Yiqing Lin, Graham B. Jones, and Irving H. Goldberg. "Probing DNA Bulges with Designed Helical Spirocyclic Molecules†." Biochemistry 46, no. 2 (January 2007): 561–67. http://dx.doi.org/10.1021/bi061744d.
Повний текст джерелаG. Keller, Sascha, Mako Kamiya, and Yasuteru Urano. "Recent Progress in Small Spirocyclic, Xanthene-Based Fluorescent Probes." Molecules 25, no. 24 (December 16, 2020): 5964. http://dx.doi.org/10.3390/molecules25245964.
Повний текст джерелаHolovatiuk, V. M., O. A. Brazhko та V. I. Kashkovsky. "ВИВЧЕННЯ ГОСТРОЇ ТОКСИЧНОСТІ ТА АНАЛГЕТИЧНОЇ АКТИВНОСТІ НОВИХ СПІРОЦИКЛІЧНИХ ПОХІДНИХ ПІРАЗОЛІДИН-3,5-ДІОНУ". Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University 6, № 3 (4 листопада 2016): 149–53. http://dx.doi.org/10.15421/201681.
Повний текст джерелаInnocenti, Riccardo, Elena Lenci, Gloria Menchi, and Andrea Trabocchi. "Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones." Beilstein Journal of Organic Chemistry 16 (February 12, 2020): 200–211. http://dx.doi.org/10.3762/bjoc.16.23.
Повний текст джерелаChernyshov, Vladimir V., Yuri V. Gatilov, Olga I. Yarovaya, Igor P. Koskin, Spartak S. Yarovoy, Konstantin A. Brylev, and Nariman F. Salakhutdinov. "The first example of the stereoselective synthesis and crystal structure of a spirobicycloquinazolinone based on (–)-fenchone and anthranilamide." Acta Crystallographica Section C Structural Chemistry 75, no. 12 (November 26, 2019): 1675–80. http://dx.doi.org/10.1107/s2053229619015766.
Повний текст джерелаLinden, Anthony, Grzegorz Mlostoń, Paulina Grzelak, and Heinz Heimgartner. "Chemo- and regioselective [3 + 2]-cycloadditions of thiocarbonyl ylides: crystal structures of trans-8-benzoyl-1,1,3,3-tetramethyl-7-trifluoromethyl-5-thiaspiro[3.4]octan-2-one and trans-3-benzoyl-2,2-diphenyl-4-(trifluoromethyl)tetrahydrothiophene." Acta Crystallographica Section E Crystallographic Communications 74, no. 12 (November 6, 2018): 1705–9. http://dx.doi.org/10.1107/s2056989018015335.
Повний текст джерелаДисертації з теми "Spirocyclic molecules"
Gilles, Laure. "Découverte et synthèse chimique d'odorants par des technologies innovantes." Electronic Thesis or Diss., Université Côte d'Azur, 2022. http://www.theses.fr/2022COAZ4100.
Повний текст джерелаThe perfumery industry in under constant pressure from national and international regulatory bodies as well and the demands of consumers to produce novel and safe organoleptic molecules via methods which are both durable and innovative. This constant drive for innovation pushes researchers towards diverse domains of the plant kingdom which contains numerous complex natural substances (CNS). At present these natural products are a source of ingredients, however, they are equally a source of inspiration for the chemist who may identify structures of interest to be synthesised with a high degree of control (chirality, quantity, quality, consistency), as well as structural analogues to provide an improvement of the olfactory properties (notes, intensity).This manuscript presents an extended analysis of the distillate of a concrete of the plant Ocimum gratissimum via GC-O complemented with GC-MS analysis. This study has also enlighted the chemical composition of the extract, characterisation of the poorly described (E)-methyl cinnamate chemotype, olfactory evaluation by a master perfumer and the identification of the principal olfactive compounds. This work simultaneously explores multistep asymmetric synthetic strategies in the aim of obtaining the different enantiomers of vetispira-2(11),6-dien-14-al. This compound is known to be an important component of agar wood essential oil and largely responsible for its particular odour. Currently no syntheses of this compound have been published. An FeCl3 catalysed acetylation of α,β-unsaturated compounds was optimised and applied to the synthesis of 24 different heterocyclic spirocycles, which are to be submitted to a master perfumer for the evaluation of their notes and olfactory interest
Kujawa, Szymon. "Rapid generation of molecular complexity under Pd(II) and Rh(III) catalysis." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/11697.
Повний текст джерелаFinne, Anna. "Novel Possibilities for Advanced Molecular Structure Design for Polymers and Networks." Doctoral thesis, KTH, Polymerteknologi, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3623.
Повний текст джерелаQC 20100602
Частини книг з теми "Spirocyclic molecules"
Cuevas-Yañez, Erick, M. V. Basavanag Unnamatla, Marco A. García-Eleno, and Subhendu Chakroborty. "Systems With a Spirocyclic Heteroatom." In Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-409547-2.14961-3.
Повний текст джерела