N-vinyl and N-unsubstituted β-lactams from 1-substituted 2-aza-1, 3-butadienes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Asymmetric synthesis of (1'R,3R,4R)-4-acetoxy-3-[1'-((tert-butyldimethylsilyl)oxy)ethyl]-2-azetidinone and other 3-(1'-hydroxyethyl)-2-azetidinones from (S)-(+)-ethyl 3-hydroxybutanoate: formal total synthesis of (+)-thienamycin
2. Studies on lactams. 81. Enantiospecific synthesis and absolute configuration of substituted .beta.-lactams from D-glyceraldehyde acetonide
3. 2-aza-1,3-dienes as novel precursors for the synthesis of -unsubstituted β-lactams. A three step synthesis of 4-acetoxy-3-phenoxy-2-azeridinone
4. The synthesis and reactions of 4-carbomethoxy β-sultams
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