Recent advances in the synthetic elaboration of sultones
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
New methods for the elaboration of sultones enable a short and highly stereoselective synthesis of methyl nonactate and establish vinylsulfonyl chloride as an allene equivalent for the intramolecular Diels-Alder reaction.
Details
Original language | English |
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Pages (from-to) | 345-346 |
Number of pages | 2 |
Journal | Phosphorus, sulfur, and silicon and the related elements |
Volume | 120-121 |
Publication status | Published - 1997 |
Peer-reviewed | Yes |
Externally published | Yes |
External IDs
ORCID | /0000-0001-8423-6173/work/171062636 |
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Keywords
ASJC Scopus subject areas
Keywords
- Desulfurization, Methyl nonactate, Methylenation, Sultones