34631-59-9Relevant academic research and scientific papers
Visible-Light-Driven, Palladium-Catalyzed Heck Reaction of Internal Vinyl Bromides with Styrenes
Li, Yunlong,Liu, Haibo,Huang, Zilong,He, Yuan,Xu, Bao-Hua,Wang, Hongmei,Yu, Zhengkun
, p. 8402 - 8413 (2021/06/28)
Functionalized 1,3-dienes were efficiently accessed from visible-light-driven, palladium-catalyzed Heck reaction of S,S-functionalized internal vinyl bromides with styrenes under mild conditions. This Heck reaction showcased tolerance of a wide array of f
Synthesis of densely substituted 1,3-butadienes through acid-catalyzed alkenylations of α-oxoketene dithioacetals with aldehydes
Liu, Changhui,Gu, Yanlong
, p. 9619 - 9627 (2015/01/09)
Aldehydes were proved to be viable reagents for implementing alkenylation of α-oxoketene dithioacetals. AlCl3 was found to be the best catalyst. The established reaction opened an avenue to access densely substituted 1,3-butadiene derivatives. The obtained product bears multiple reactive sites that can be converted into various valuable molecules. (Chemical Equation Presented).
Synthesis of 2,3,5-trisubstituted furans from α-formylaroylketene dithioacetals
Sasikala,Kalesh,Anabha,Pillai, P. Madhavan,Asokan,Devaky
experimental part, p. 1667 - 1669 (2011/04/25)
A new strategy for the synthesis of 2,3,5-trisbustituted furans from α-formylketene dithioacetals is described. The protocol involves a facile conversion of α-formylketene dithioacetals to vinylketene dithioacetals via Wittig reaction and subsequent N-bro
