Thieme Chemistry Journal Awardees - Where Are They Now? Diastereoselective Tandem Iodocarbonate Cyclization of 1,5-Enynes

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초록

A diastereoselective, metal-free tandem iodocarbonate-cyclization of 1,5-enyne, emulating the reactivity of gold catalysis is described. The normal selectivity of iodonium reagents for alkene is reversed favoring alkyne activation in the presence of aryl alkynes.

키워드

enynesiodocyclizationIBrtandem reactionsdiastereoselectivityCATALYZED CASCADE REACTIONSTERT-BUTYL CARBONATESGOLD(I)-CATALYZED FORMATIONORGANIC-SYNTHESISDOMINO REACTIONSGOLDCYCLOISOMERIZATIONENYNESIONSN'-(2-ALKYNYLBENZYLIDENE)HYDRAZIDES
제목
Thieme Chemistry Journal Awardees - Where Are They Now? Diastereoselective Tandem Iodocarbonate Cyclization of 1,5-Enynes
저자
Lim, ChoongminRao, M. SheshaShin, Seunghoon
DOI
10.1055/s-0029-1219183
발행일
2010-02
유형
Article
저널명
Synlett
3
페이지
368 ~ 373