ChemInform Abstract: Au(III)-Catalyzed Ring Opening Reaction of 1-Cyclopropyl-2-yn-1-ols with Nucleophiles: Highly Efficient Approach to (Z)-Conjugated Enynes.

ChemInform ◽  
2008 ◽  
Vol 39 (21) ◽  
Author(s):  
Hui-quan Xiao ◽  
Xing-zhong Shu ◽  
Ke-gong Ji ◽  
Chen-ze Qi ◽  
Yong-min Liang
Keyword(s):  
Ring Opening ◽  
Efficient Approach ◽  
Highly Efficient ◽  
Ring Opening Reaction ◽  
Conjugated Enynes

Au(iii)-catalyzed ring opening reaction of 1-cyclopropyl-2-yn-1-ols with nucleophiles: highly efficient approach to (Z)-conjugated enynes

2007 ◽  
Vol 31 (12) ◽  
pp. 2041 ◽  
Author(s):  
Hui-quan Xiao ◽  
Xing-zhong Shu ◽  
Ke-gong Ji ◽  
Chen-ze Qi ◽  
Yong-min Liang
Keyword(s):  
Ring Opening ◽  
Efficient Approach ◽  
Highly Efficient ◽  
Ring Opening Reaction ◽  
Conjugated Enynes

scholarly journals Preparation of a highly efficient Pt/USY catalyst for hydrogenation and selective ring-opening reaction of tetralin

2018 ◽  
Vol 15 (3) ◽  
pp. 605-612 ◽  
Author(s):  
Qi Wang ◽  
Zhang-Gui Hou ◽  
Bo Zhang ◽  
Jian Liu ◽  
Wei-Yu Song ◽  
...  
Keyword(s):  
Ring Opening ◽  
Highly Efficient ◽  
Ring Opening Reaction ◽  
Selective Ring Opening

Ir-Catalyzed ring-opening of oxa(aza)benzonorbornadienes with water or alcohols

2019 ◽  
Vol 6 (8) ◽  
pp. 1151-1156 ◽  
Author(s):  
Xin Yang ◽  
Wen Yang ◽  
Yongqi Yao ◽  
Yingying Deng ◽  
Dingqiao Yang
Keyword(s):  
Ring Opening ◽  
Highly Efficient ◽  
Ring Opening Reaction

A highly efficient Ir-catalyzed ring-opening reaction of oxa(aza)benzonorbornadienes with water was firstly developed, which afforded a mild access to substituted dihydronaphthalene products with excellent yields (up to 99%) within 30 min.

An efficient approach to gem-difluorocyclopropylstannanes via highly regio- and stereoselective hydrostannylation of gem-difluorocyclopropenes and their unique ring-opening reaction to afford β-fluoroallylic alcohols

2015 ◽  
Vol 13 (12) ◽  
pp. 3721-3731 ◽  
Author(s):  
T. Nihei ◽  
T. Hoshino ◽  
T. Konno
Keyword(s):  
Ring Opening ◽  
Efficient Approach ◽  
Ring Opening Reaction

gem-Difluorocyclopropylstannanes, prepared via the hydrostannylation of gem-difluorocyclopropenes, were treated with MeLi and then quenching agents, to give (Z)-β-fluoroallyllic alcohols, ethers, esters, and amides.

A facile ring opening reaction of furfuryl selenides. Highly efficient method for dienones

1980 ◽  
Vol 21 (33) ◽  
pp. 3209-3212 ◽  
Author(s):  
Isao Kuwajima ◽  
Showay Hoshino ◽  
Toshihiko Tanaka ◽  
Makoto Shimizu
Keyword(s):  
Efficient Method ◽  
Ring Opening ◽  
Highly Efficient ◽  
Ring Opening Reaction
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