Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Andrei V. Maskaev"'
Autor:
M. I. Lazareva, William A. Smit, Dmitriy S. Chekmarev, Georgy V. Zatonsky, Andrei V. Maskaev, R. Caple
Publikováno v:
The Journal of Organic Chemistry. 67:7957-7967
Data on the selectivity of the Lewis acids induced transformations of the title compounds are presented, and the routes leading to formation of products containing either cyclohexane or 1,3-diene units are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce684a8466624d4518a02801a3645fba
https://doi.org/10.1021/jo0261202
https://doi.org/10.1021/jo0261202
Autor:
M. I. Lazareva, Georgy V. Zatonsky, R. Caple, Andrei V. Maskaev, Dmitrii S. Chekmarev, William A. Smit
Publikováno v:
Mendeleev Communications. 11:176-178
The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the formation of substituted cyclohexane or 1,3-diene derivatives, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90958927986283765af7beeffc113c91
https://doi.org/10.1070/mc2001v011n05abeh001513
https://doi.org/10.1070/mc2001v011n05abeh001513
Autor:
Andrei V. Maskaev, Georgy V. Zatonsky, R. Caple, M. I. Lazareva, Dmitrii S. Chekmarev, William A. Smit
Publikováno v:
ChemInform. 33
The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the formation of substituted cyclohexane or 1,3-diene derivatives, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da185e1b15274b7143bc454cf4132b48
https://doi.org/10.1002/chin.200211078
https://doi.org/10.1002/chin.200211078