scholarly journals Stereoselective Synthesis of δ-Lactones from 5-Oxoalkanals via One-Pot Sequential Acetalization, Tishchenko Reaction, and Lactonization by Cooperative Catalysis of Samarium Ion and Mercaptan

2001 ◽  
Vol 66 (25) ◽  
pp. 8573-8584 ◽  
Author(s):  
Jue-Liang Hsu ◽  
Jim-Min Fang
Author(s):  
Yuan Li ◽  
Jin Wu ◽  
Hui Li ◽  
Qian Sun ◽  
Lixue Xiong ◽  
...  

An efficient one-pot method for the synthesis of (Z,Z)-isomers of 1,4-bis(sulfanyl)-1,4-diaryl-1,3-butadienes by the cooperative catalysis of Cu(Xantphos)I/Pd(OAc)2 and a base has been developed.


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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