Mild and selective boronic acid catalyzed 1,3-transposition of allylic alcohols and Meyer–Schuster rearrangement of propargylic alcohols

2011 ◽  
Vol 2 (7) ◽  
pp. 1305 ◽  
Author(s):  
Hongchao Zheng ◽  
Michal Lejkowski ◽  
Dennis G. Hall
ChemInform ◽  
2010 ◽  
Vol 41 (22) ◽  
pp. no-no
Author(s):  
J. Adam McCubbin ◽  
Hamidreza Hosseini ◽  
Oleg V. Krokhin

2010 ◽  
Vol 75 (3) ◽  
pp. 959-962 ◽  
Author(s):  
J. Adam McCubbin ◽  
Hamidreza Hosseini ◽  
Oleg V. Krokhin

2018 ◽  
Vol 140 (10) ◽  
pp. 3644-3651 ◽  
Author(s):  
Masamichi Tanaka ◽  
Akira Nakagawa ◽  
Nobuya Nishi ◽  
Kiyoko Iijima ◽  
Ryuichi Sawa ◽  
...  

2011 ◽  
Vol 52 (19) ◽  
pp. 2465-2467 ◽  
Author(s):  
Rogelio P. Frutos ◽  
Thomas Tampone ◽  
Jason A. Mulder ◽  
Yibo Xu ◽  
Diana Reeves ◽  
...  
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Synlett ◽  
2009 ◽  
Vol 2009 (12) ◽  
pp. 1985-1989 ◽  
Author(s):  
Roberto Sanz ◽  
Mukut Gohain ◽  
Delia Miguel ◽  
Alberto Martínez ◽  
Félix Rodríguez

Synlett ◽  
2019 ◽  
Vol 30 (03) ◽  
pp. 356-360 ◽  
Author(s):  
Manickavasakam Ramasamy ◽  
Hui-Chang Lin ◽  
Sheng-Chu Kuo ◽  
Min-Tsang Hsieh

A practical Lewis acid-catalyzed Meyer–Schuster rearrangement of fluoroalkylated propargylic alcohols, leading to a series of β-fluoroalkyl-α,β-enones, is developed. The methodology reported herein features moderate to high yields and high stereoselectivity in the synthesis of β-alkyl-β-fluoroalkyl-α,β-enones.


ChemInform ◽  
2011 ◽  
Vol 42 (35) ◽  
pp. no-no
Author(s):  
Mang Wang ◽  
Shaoguang Sun ◽  
Deqiang Liang ◽  
Bangyu Liu ◽  
Ying Dong ◽  
...  

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