One-Pot Stereoselective Synthesis of (Z)-β-Ketoenamides from β-Halo α,β-Unsaturated Aldehydes

2014 ◽  
Vol 2014 (16) ◽  
pp. 3483-3490 ◽  
Author(s):  
Junali Gogoi ◽  
Pranjal Gogoi ◽  
Romesh C. Boruah
Author(s):  
Sundarababu Baskaran ◽  
Kirana D V ◽  
Kanak Kanti Das

A one-pot catalytic method has been developed for the stereoselective synthesis of cyclopropane-fused cyclic amidines using CuBr2/K2S2O8 as an efficient single electron transfer (SET) oxidative system. The generality of this...


RSC Advances ◽  
2021 ◽  
Vol 11 (24) ◽  
pp. 14755-14768
Author(s):  
Malihe Akhavan ◽  
Ahmadreza Bekhradnia

An efficient, green, one-pot, and three-component protocol has been reported for the stereoselective synthesis of a new class of spiro thiazolidines.


Tetrahedron ◽  
1997 ◽  
Vol 53 (38) ◽  
pp. 13139-13148 ◽  
Author(s):  
Tahir M. Kasumov ◽  
Namig Sh. Pirguliyev ◽  
Valery K. Brel ◽  
Yuri K. Grishin ◽  
Nikolai S. Zefirov ◽  
...  

2021 ◽  
Vol 08 ◽  
Author(s):  
Chithaluri Sudhakar ◽  
Pochamoni Ramudu

: An efficient stereoselective synthesis of 2,6-disubstituted-4-thiocyanatotetrahydropyrans has been developed through a one pot three-component reaction of aldehydes, trimethyl allylsilane and NH4SCN in the presence of BF3.Et2O at room temperature. The products are formed rapidly (10-30 min) in excellent yields (78-98%).


ChemInform ◽  
2005 ◽  
Vol 36 (28) ◽  
Author(s):  
Seiichi Inoue ◽  
Ping Wang ◽  
Mami Nagao ◽  
Yujiro Hoshino ◽  
Kiyoshi Honda

ChemInform ◽  
2010 ◽  
Vol 31 (6) ◽  
pp. no-no
Author(s):  
Teruaki Mukaiyama ◽  
Yoshinari Wakiyama ◽  
Kazuo Miyazaki ◽  
Kazuya Takeuchi

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