Letteratura scientifica selezionata sul tema "Spirocyclic molecules"
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Articoli di riviste sul tema "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, n. 34 (2021): 11294–305. http://dx.doi.org/10.1039/d1sc03615g.
Benabdallah, Mohammed, Oualid Talhi, Fatiha Nouali, Nouredine Choukchou-Braham, Khaldoun Bachari e Artur M. S. Silva. "Advances in Spirocyclic Hybrids: Chemistry and Medicinal Actions". Current Medicinal Chemistry 25, n. 31 (16 ottobre 2018): 3748–67. http://dx.doi.org/10.2174/0929867325666180309124821.
Paquette, Leo A. "Spirocyclic Restriction of Nucleosides". Australian Journal of Chemistry 57, n. 1 (2004): 7. http://dx.doi.org/10.1071/ch03267.
Shen, Guo-Liang, Jing Sun e 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, n. 6 (2015): 4475–83. http://dx.doi.org/10.1039/c4ra13760d.
Kappen, Lizzy S., Yiqing Lin, Graham B. Jones e Irving H. Goldberg. "Probing DNA Bulges with Designed Helical Spirocyclic Molecules†". Biochemistry 46, n. 2 (gennaio 2007): 561–67. http://dx.doi.org/10.1021/bi061744d.
G. Keller, Sascha, Mako Kamiya e Yasuteru Urano. "Recent Progress in Small Spirocyclic, Xanthene-Based Fluorescent Probes". Molecules 25, n. 24 (16 dicembre 2020): 5964. http://dx.doi.org/10.3390/molecules25245964.
Holovatiuk, V. M., O. A. Brazhko e 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, n. 3 (4 novembre 2016): 149–53. http://dx.doi.org/10.15421/201681.
Innocenti, Riccardo, Elena Lenci, Gloria Menchi e Andrea Trabocchi. "Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones". Beilstein Journal of Organic Chemistry 16 (12 febbraio 2020): 200–211. http://dx.doi.org/10.3762/bjoc.16.23.
Chernyshov, Vladimir V., Yuri V. Gatilov, Olga I. Yarovaya, Igor P. Koskin, Spartak S. Yarovoy, Konstantin A. Brylev e 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, n. 12 (26 novembre 2019): 1675–80. http://dx.doi.org/10.1107/s2053229619015766.
Linden, Anthony, Grzegorz Mlostoń, Paulina Grzelak e 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, n. 12 (6 novembre 2018): 1705–9. http://dx.doi.org/10.1107/s2056989018015335.
Tesi sul tema "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.
The 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.
Finne, 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.
QC 20100602
Capitoli di libri sul tema "Spirocyclic molecules":
Cuevas-Yañez, Erick, M. V. Basavanag Unnamatla, Marco A. García-Eleno e 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.