Selective formation of 1,3,4-trisubstituted and 3,4-disubstituted trans-β-lactams from zinc enolates and imines
- 1 January 1987
- journal article
- research article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 106 (9), 516-518
- https://doi.org/10.1002/recl.19871060910
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Reactivity of 1-aza-4-oxo-1,3-butadienes (.alpha.-imino ketones) toward diorganozinc reagents: regio- and chemoselective transfer of organo groups in the ZnR2/R1N:C(R2)C(R3):O system and x-ray structure of [cyclic] [EtZn(Et)(tert-Bu)NC(H):C(Me)O]2Organometallics, 1987
- The unexpected formation of trans‐β‐lactams in the reaction of α‐iminoesters (R-NC(H)C(O)OR′) with diethylzinc. Crystal structure of trans‐1‐(N‐t‐butyl)‐3‐(N‐t‐butyl‐N‐ethylamino)‐4‐ methoxycarbonylazetidin‐2‐oneRecueil des Travaux Chimiques des Pays-Bas, 1987
- .beta.-Lactams from esters and sulfenimines: a new route to monobactamsThe Journal of Organic Chemistry, 1986
- A convenient synthesis of 4-unsubstituted .beta.-lactamsJournal of the American Chemical Society, 1985
- Preparation of primary amines and 2-azetidinones via N-(trimethylsilyl)iminesThe Journal of Organic Chemistry, 1983
- Preparation of .beta.-lactams by the condensation of lithium ester enolates with aryl aldiminesThe Journal of Organic Chemistry, 1980
- Stereochemistry in the β-lactam series—IIITetrahedron, 1968