Lewis Acid Mediated Tandem Reaction of Propargylic Alcohols with Hydroxylamine Hydrochloride To Give α,β-Unsaturated Amides and Alkenyl Nitriles

2015 ◽  
Vol 80 (18) ◽  
pp. 9200-9207 ◽  
Author(s):  
Ya-Ping Han ◽  
Xian-Rong Song ◽  
Yi-Feng Qiu ◽  
Xin-Hua Hao ◽  
Jia Wang ◽  
...  
2014 ◽  
Vol 20 (38) ◽  
pp. 12046-12050 ◽  
Author(s):  
Xian-Rong Song ◽  
Ya-Ping Han ◽  
Yi-Feng Qiu ◽  
Zi-Hang Qiu ◽  
Xue-Yuan Liu ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (11) ◽  
pp. no-no
Author(s):  
Xian-Rong Song ◽  
Ya-Ping Han ◽  
Yi-Feng Qiu ◽  
Zi-Hang Qiu ◽  
Xue-Yuan Liu ◽  
...  

2018 ◽  
Vol 16 (5) ◽  
pp. 756-764 ◽  
Author(s):  
Sengodagounder Muthusamy ◽  
Alagesan Balasubramani ◽  
Eringathodi Suresh

The BF3·Et2O catalyzed tandem reaction of nitrosobenzenes and propargylic alcohols for the formation of highly substituted indole-3-carbinols.


Synlett ◽  
2011 ◽  
Vol 2011 (08) ◽  
pp. 1179-1183 ◽  
Author(s):  
Zhuang-ping Zhan ◽  
Min Lin ◽  
Qing-zhen Chen ◽  
Yu Zhu ◽  
Xin-liang Chen ◽  
...  

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.


Tetrahedron ◽  
2016 ◽  
Vol 72 (44) ◽  
pp. 6935-6942 ◽  
Author(s):  
Qi Zhang ◽  
Linjing Zhang ◽  
Chaojun Tang ◽  
Huan Luo ◽  
Xuediao Cai ◽  
...  

2016 ◽  
Vol 18 (15) ◽  
pp. 3866-3869 ◽  
Author(s):  
Ya-Ping Han ◽  
Xian-Rong Song ◽  
Yi-Feng Qiu ◽  
Xue-Song Li ◽  
Heng-Rui Zhang ◽  
...  

2015 ◽  
Vol 51 (2) ◽  
pp. 358-361 ◽  
Author(s):  
Shan-yong Chen ◽  
Winnie Liu ◽  
Xuedan Wu ◽  
Jun Ying ◽  
Xiaoqi Yu ◽  
...  

Zn powder and EtI in the presence of (S)-BINOL and Ti(OiPr)4 promote highly enantioselective alkyne addition to aldehydes at rt to generate chiral propargylic alcohols.


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