ChemInform Abstract: Construction of Chiral α-Amino Quaternary Stereogenic Centers via Phase-Transfer Catalyzed Enantioselective α-Alkylation of α-Amidomalonates.

ChemInform ◽  
2015 ◽  
Vol 46 (32) ◽  
pp. no-no
Author(s):  
Hyeung-geun Park ◽  
et al.
RSC Advances ◽  
2016 ◽  
Vol 6 (81) ◽  
pp. 77427-77430 ◽  
Author(s):  
Min Woo Ha ◽  
Sujee Choi ◽  
Seek Kim ◽  
Jun Young Lee ◽  
Jae Kyun Lee ◽  
...  

The enantioselective synthesis of α-acyloxy-α-alkylmalonates was developed as an efficient method for producing chiral α-tertiary alcohols, which are potentially valuable intermediates in the synthesis of natural products and pharmaceuticals.


2018 ◽  
Vol 83 (2) ◽  
pp. 1011-1018 ◽  
Author(s):  
Min Woo Ha ◽  
Jun Young Lee ◽  
Doyoung Kim ◽  
Geumwoo Lee ◽  
Jae Kyun Lee ◽  
...  

2015 ◽  
Vol 80 (6) ◽  
pp. 3270-3279 ◽  
Author(s):  
Min Woo Ha ◽  
Myungmo Lee ◽  
Sujee Choi ◽  
Seek Kim ◽  
Suckchang Hong ◽  
...  

ChemInform ◽  
2016 ◽  
Vol 47 (52) ◽  
Author(s):  
Min Woo Ha ◽  
Sujee Choi ◽  
Seek Kim ◽  
Jun Young Lee ◽  
Jae Kyun Lee ◽  
...  

2014 ◽  
Vol 136 (7) ◽  
pp. 2682-2694 ◽  
Author(s):  
Ilan Marek ◽  
Yury Minko ◽  
Morgane Pasco ◽  
Tom Mejuch ◽  
Noga Gilboa ◽  
...  

Synthesis ◽  
2019 ◽  
Vol 51 (15) ◽  
pp. 2959-2964 ◽  
Author(s):  
Yoshiyasu Ichikawa ◽  
Hirofumi Morimoto ◽  
Toshiya Masuda

A new approach was developed to construct quaternary stereogenic centers bearing nitrogen substituents in an enantioselective manner. The strategy takes advantage of [1,3]-chirality transfer from a chiral primary alcohol equivalent through an allyl cyanate-to-isocyanate rearrangement. This approach was employed in an efficient eight-step synthesis of the marine natural product, (+)-geranyllinaloisocyanide, in 43% overall yield.


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