Enantioselective synthesis of α,α-difluoro-β-lactams using amino alcohol ligands

2014 ◽  
Vol 12 (33) ◽  
pp. 6484-6489 ◽  
Author(s):  
Atsushi Tarui ◽  
Takeshi Ikebata ◽  
Kazuyuki Sato ◽  
Masaaki Omote ◽  
Akira Ando

A practical and highly enantioselective Reformatsky reaction of ethyl bromodifluoroacetate with imines using a cheap and commercially available amino alcohol ligand is described.

ChemInform ◽  
2004 ◽  
Vol 35 (6) ◽  
Author(s):  
Peter Pojarliev ◽  
William T. Biller ◽  
Harry J. Martin ◽  
Benjamin List

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
K. Chandra Babu ◽  
R. Buchi Reddy ◽  
E. Naresh ◽  
K. Ram Mohan ◽  
G. Madhusudhan ◽  
...  

We report an asymmetric synthesis of (-)-Levetiracetam (1) in six steps starting from versatile new chiralN-sulfinimine (3). The key step, stereoselective 1,2-addition of ethylmagnesium bromide (EtMgBr) to chiralN-sulfinimine derived from (R)-glyceraldehyde acetonide and (S)-t-BSA, gave the corresponding sulfonamide (2) in high diastereoselectivity. Simultaneous deprotection and deacetylation followed by NaIO4cleavage and reduction gaveβ-amino alcohol (6). Subsequent reactions yielded the targeted compound levetiracetam (1).


1995 ◽  
Vol 6 (11) ◽  
pp. 2641-2642 ◽  
Author(s):  
Aiqiao Mi ◽  
Zhaoyang Wang ◽  
Zhenwan Chen ◽  
Yaozhong Jiang ◽  
Albert S.C. Chan ◽  
...  

2015 ◽  
Vol 19 (9) ◽  
pp. 1317-1322 ◽  
Author(s):  
Michael A. Schmidt ◽  
Emily A. Reiff ◽  
Xinhua Qian ◽  
Chao Hang ◽  
Vu Chi Truc ◽  
...  

1987 ◽  
Vol 16 (1) ◽  
pp. 129-132 ◽  
Author(s):  
Tamotsu Fujisawa ◽  
Hiroki Hayashi ◽  
Yoshino Kishioka

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