ChemInform Abstract: One-Pot Stereoselective Synthesis of 1,2-Amino Alcohol Derivatives.

ChemInform ◽  
2011 ◽  
Vol 42 (45) ◽  
pp. no-no
Author(s):  
Alicia Boto ◽  
Ivan Romero-Estudillo
2011 ◽  
Vol 13 (13) ◽  
pp. 3426-3429 ◽  
Author(s):  
Alicia Boto ◽  
Iván Romero-Estudillo

1995 ◽  
Vol 25 (19) ◽  
pp. 2975-2980 ◽  
Author(s):  
Robert M. Przeslawski ◽  
Suzanne Newman ◽  
Edward R. Thornton ◽  
Madeleine M. Joullié

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%).


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