Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alexey M. Kavun"'
Autor:
Yulia V. Nelyubina, Andrey G. Lvov, Anatoly V. Metelitsa, Alexey M. Kavun, Vadim V. Kachala, Valerii Z. Shirinian
Publikováno v:
The Journal of Organic Chemistry. 82:1477-1486
The effect of the size of the ethene bridge on the structural and spectral properties of photochromic diarylethenes, which remains a poorly understood phenomenon, was studied as applied to diarylethenes containing unsymmetrical (cyclohexenone and cyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0658af9ebbf72b064a586db0e6e7bb03
https://doi.org/10.1021/acs.joc.6b02665
https://doi.org/10.1021/acs.joc.6b02665
Autor:
Vadim V. Kachala, Andrey G. Lvov, Konstantin A. Lyssenko, Alexey M. Kavun, Valerii Z. Shirinian
Publikováno v:
Organicbiomolecular chemistry. 17(20)
A general strategy for the preparative benzannulation of aromatic heterocycles via photocyclization of 1,2-dihetarylethenes was proposed for the first time. The strategy includes two steps, namely, modular assembly of dihetarylethenes from widely ava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f01136f272b33e0083c14dd1615a22e
https://pubmed.ncbi.nlm.nih.gov/30964495
https://pubmed.ncbi.nlm.nih.gov/30964495
Publikováno v:
Synthesis. 49:1255-1263
A new efficient method was developed for the synthesis of triaryl-substituted cyclohexenones and salicylates. The method is based on the Robinson annulation of readily available keto esters and chalcones, followed by the aromatization of the cyclohex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73609297c0297b8093c4580a4c5f834a
https://doi.org/10.1055/s-0036-1588908
https://doi.org/10.1055/s-0036-1588908
Autor:
Dmitry V. Lonshakov, Valerii Z. Shirinian, Alexey M. Kavun, Anton V. Yadykov, Andrey G. Lvov, Mikhail M. Krayushkin
Publikováno v:
Dyes and Pigments. 124:258-267
New dialkylamino groups-comprising diarylethenes of 2,3-diarylcyclopent-2-en-1-one (DCP) series have been synthesized and its photochromic, fluorescent as well as acidochromic features have been investigated. It was shown that photochromic properties
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75c5cabf5a2e960a067460be5a6b3df6
https://doi.org/10.1016/j.dyepig.2015.09.027
https://doi.org/10.1016/j.dyepig.2015.09.027
Publikováno v:
Mendeleev Communications. 24:277-279
Alkylation of ethyl 4-(2,5-dimethylthiophen-3-yl)-3-oxobutanoate with 2-aryl-4-bromoacetyl-5-methyl-1,3-oxazole followed by decar-boxylation–cyclization of the intermediate diketo ester affords the title photochromic compounds. Relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73256e051888e54871663a20df5c82e0
https://doi.org/10.1016/j.mencom.2014.09.010
https://doi.org/10.1016/j.mencom.2014.09.010
Publikováno v:
ChemInform. 46
Novel unsymmetrical photochromic diarylethenes of the cyclopentenone series are synthesized and their photospectroscopic properties are investigated in MeCN.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96042f4335d43e545980c43071b9e12d
https://doi.org/10.1002/chin.201511169
https://doi.org/10.1002/chin.201511169
Autor:
Igor V. Zavarzin, Valerii Z. Shirinian, Vadim V. Kachala, Andrey G. Lvov, Alexey M. Kavun, Mikhail M. Krayushkin
Publikováno v:
ChemInform. 46
The photocyclization/rearrangement reaction of diarylethenes provides various substituted naphthalene derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e27b3436875e78257e397daa0869e028
https://doi.org/10.1002/chin.201509117
https://doi.org/10.1002/chin.201509117
Autor:
Vadim V. Kachala, Alexey M. Kavun, Mikhail M. Krayushkin, Andrey G. Lvov, Igor V. Zavarzin, Valerii Z. Shirinian
Publikováno v:
Organic letters. 16(17)
A novel photochemical rearrangement of diarylethenes bearing oxazole and benzene derivatives as aryl moieties that results in the formation of polyaromatic systems was investigated. The mechanism of the transformation includes photocyclization, seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd1947f59582864abd72fddb9414351
https://pubmed.ncbi.nlm.nih.gov/25115452
https://pubmed.ncbi.nlm.nih.gov/25115452