Catalytic Asymmetric Aza-Henry Addition to Imino Esters

Author(s):  
R. M. Garbaccio ◽  
S. E. Wolkenberg
2003 ◽  
Vol 5 (14) ◽  
pp. 2481-2484 ◽  
Author(s):  
Yoshitaka Nakamura ◽  
Ryosuke Matsubara ◽  
Hiroshi Kiyohara ◽  
Shū Kobayashi

2010 ◽  
Vol 132 (15) ◽  
pp. 5338-5339 ◽  
Author(s):  
Takayoshi Arai ◽  
Asami Mishiro ◽  
Naota Yokoyama ◽  
Kuniko Suzuki ◽  
Hiroyasu Sato

ChemInform ◽  
2003 ◽  
Vol 34 (46) ◽  
Author(s):  
Yoshitaka Nakamura ◽  
Ryosuke Matsubara ◽  
Hiroshi Kiyohara ◽  
Shu Kobayashi

2006 ◽  
Vol 78 (2) ◽  
pp. 267-274 ◽  
Author(s):  
Jian-Xin Ji ◽  
Jing Wu ◽  
Lijin Xu ◽  
Chiu-Wing Yip ◽  
Kim Hung Lam ◽  
...  

Optically active tertiary aminonaphthol ligands were obtained by a new, convenient procedure and were found to catalyze the enantioselective alkenyl and phenyl transfer to aldehydes in high yields and excellent enantiomeric excesses (ee's). The catalytic asymmetric introduction of alkynyl functionality to α-amino acid derivatives was realized by the direct addition of terminal alkynes to α-imino ester in the presence of chiral copper(I) complex under mild reaction conditions.


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