Reaction of α-azidoketones with highly stabilized michael acceptors: A new synthesis of densely functionalized pyrroles
✍ Scribed by JoséL Marco; Angeles Martínez-Grau; Nazario Martín; Carlos Seoane
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 190 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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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
A haloboration adduct, formed by the reaction of B-iodo-9-borabicyclo[3.3. llnonanes with ethoxyethyne reacts with aldehydes chemoselectively under very mild conditions. The subsequent hydrolytic work-up affords--a&unsaturated esters in good yields. The transformation of aldehydes to two carbon-ho