The Diels–Alder Cyclization of Ketenimines
Author:
Affiliation:
1. Department of Chemistry, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol300742t
Reference66 articles.
1. Entropic Intermediates and Hidden Rate-Limiting Steps in Seemingly Concerted Cycloadditions. Observation, Prediction, and Origin of an Isotope Effect on Recrossing
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3. Catalytic, asymmetric reactions of ketenes and ketene enolates
4. Preparation of β-lactams by [2+2] cycloaddition of ketenes and imines
5. The Mechanism of the Ketene−Imine (Staudinger) Reaction in Its Centennial: Still an Unsolved Problem?
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