Simple and practical one-step synthesis of new 1,3-dienic δ-sultones from terminal alkynes and some synthetic applications of these compounds; Journal of Sulfur Chemistry; Vol. 32, iss. 1

Библиографические подробности
Источник:Journal of Sulfur Chemistry
Vol. 32, iss. 1.— 2011.— [P. 3-16]
Другие авторы: Gaitzsch J. Jens, Rogachev V. O. Victor Olegovich, Metz Р. Peter, Filimonov V. D. Viktor Dmitrievich, Zahel М. Martin, Kataeva О. Olga
Примечания:Title screen
1,3-Dienic δ -sultones 4,6-diaryl-[1,2]oxathiine 2,2-dioxides were synthesized via a one-step reaction of arylalkynes with dioxane sulfotrioxide. The reactivity of various alkynes in this reaction was investigated. The resulting sultones were brominated with Br2 or N-bromosuccinimide regioselectively α to sulfur and subsequently coupled with phenylacetylene using Sonogashira conditions
Режим доступа: по договору с организацией-держателем ресурса
Язык:английский
Опубликовано: 2011
Предметы:
Online-ссылка:http://dx.doi.org/10.1080/17415993.2010.537339
Формат: Электронный ресурс Статья
Запись в KOHA:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=636568
Описание
Примечания:Title screen
1,3-Dienic δ -sultones 4,6-diaryl-[1,2]oxathiine 2,2-dioxides were synthesized via a one-step reaction of arylalkynes with dioxane sulfotrioxide. The reactivity of various alkynes in this reaction was investigated. The resulting sultones were brominated with Br2 or N-bromosuccinimide regioselectively α to sulfur and subsequently coupled with phenylacetylene using Sonogashira conditions
Режим доступа: по договору с организацией-держателем ресурса
DOI:10.1080/17415993.2010.537339