Catalytic Asymmetric Michael Addition/Cyclization of Isothiocyanato Oxindoles: Highly Efficient and Versatile Approach for the Synthesis of 3,2′-Pyrrolidinyl Mono- and Bi-spirooxindole Frameworks

2012 ◽  
Vol 19 (4) ◽  
pp. 1184-1188 ◽  
Author(s):  
Yi-Ming Cao ◽  
Fang-Fang Shen ◽  
Fu-Ting Zhang ◽  
Rui Wang
ChemInform ◽  
2010 ◽  
Vol 29 (52) ◽  
pp. no-no
Author(s):  
K. FUNABASHI ◽  
Y. SAIDA ◽  
M. KANAI ◽  
T. ARAI ◽  
H. SASAI ◽  
...  

Author(s):  
Irishi N. N. Namboothiri ◽  
Meeta Bhati ◽  
Madhu Ganesh ◽  
Basavaprabhu Hosamani ◽  
Thekke V. Baiju ◽  
...  

2015 ◽  
Vol 51 (49) ◽  
pp. 9979-9982 ◽  
Author(s):  
Jin-Miao Tian ◽  
Yong-Hai Yuan ◽  
Yong-Qiang Tu ◽  
Fu-Min Zhang ◽  
Xiao-Bo Zhang ◽  
...  

A novel chiral spiro-pyrrolidine silyl ether organocatalyst has been designed and applied to an asymmetric Michael addition reaction.


ChemInform ◽  
2009 ◽  
Vol 40 (2) ◽  
Author(s):  
Zhigang Yang ◽  
Jie Liu ◽  
Xiaohua Liu ◽  
Zhen Wang ◽  
Xiaoming Feng ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 26 (14) ◽  
pp. no-no
Author(s):  
M. YAMAGUCHI ◽  
T. SHIRAISHI ◽  
Y. IGARASHI ◽  
M. HIRAMA

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