Reaction of N-trialkylsilylimines with a variety of glycine-derived ketenes produced 1,3-azadienes, which in some cases have been isolated and characterised. A conrotatory ring closure of these compounds gave rise to the formation of the azetidine-2-ones, thus allowing a formal two-step Staudinger r
ChemInform Abstract: Stereochemical Aspects of a Two-Step Staudinger Reaction — Asymmetric Synthesis of Chiral Azetidine-2-ones.
✍ Scribed by Alessandro Bongini; Mauro Panunzio; Giovanni Piersanti; Elisa Bandini; Giorgio Martelli; Giuseppe Spunta; Alessandro Venturini
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 38 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v