C4,C4‘-Bis-β-lactam to Fused Bis-γ-lactam Rearrangement
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (26) , 9156-9163
- https://doi.org/10.1021/jo960826c
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Stereoselective Synthesis of Vinyl Ethers by the Reaction of N-(Arylidene(or alkylidene)amino)-2-azetidinones with OzoneThe Journal of Organic Chemistry, 1995
- Preparation of .alpha.-Methylene and .alpha.-Ethylidene .beta.-Lactams via the Ester Enolate-Imine Condensation Using .beta.-(Dialkylamino) Esters as Starting Materials: Scope and Synthetic ApplicationsThe Journal of Organic Chemistry, 1994
- Efficient Asymmetric Synthesis of cis-4-Formyl .beta.-Lactams from L-(+)-Tartaric AcidThe Journal of Organic Chemistry, 1994
- New reactivity patterns of the .beta.-lactam ring: tandem C3-C4 bond breakage-rearrangement of 4-acyl- or 4-imino-3,3-dimethoxy-2-azetidinones promoted by stannous chloride (SnCl2-2H2O)The Journal of Organic Chemistry, 1993
- The Wittig Reaction of Moncyclic β-LactamsSynlett, 1993
- Stereoselective preparation of mono- and bis-.beta.-lactams by the 1,4-diaza-1,3-diene - acid chloride condensation: scope and synthetic applicationsThe Journal of Organic Chemistry, 1992
- Conversion of Beta-Lactams to Versatile Synthons via Molecular Rearrangement and Lactam CleavageHETEROCYCLES, 1988
- Remarkable effects of lone pair-lone pair interactions on the extremely stereoselective [2 + 2] cycloaddition of azidoketene to chiral 3-imino-.beta.-lactamsJournal of the American Chemical Society, 1987
- An Enantioselective β‐Lactam Synthesis Starting from L‐(S)‐Glyceraldehyde AcetonideHelvetica Chimica Acta, 1983
- Effective method for the asymmetric synthesis of bis-β-lactams by the cycloaddition of azidoketen to benzylideneamines bearing a chiral β-lactam backboneJournal of the Chemical Society, Chemical Communications, 1981