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Regio‐ and Diastereoselective Dimerization of Diazo Carbonyls: A Cooperative Catalytic Approach to Complex Scaffolds with Four Contiguous Stereocenters.
- Source :
-
Chemistry - A European Journal . Sep2020, Vol. 26 Issue 49, p11119-11123. 5p. - Publication Year :
- 2020
-
Abstract
- Starting from readily available o‐diazoacyl‐substituted arene carboxylates, scaffolds with the 5,9‐epoxycyclohepta[b]pyran‐2(3H)‐one core were obtained by cooperative RhII, Lewis and Brønsted acid catalysis. Four new bonds, three functional groups (lactone, ketal, and alcohol) and four contiguous stereocenters are formed during this regio‐ and diastereoselective process in a single synthetic step. Intensive optimization and mechanistic studies, including the trapping, isolation, and elucidation of reaction intermediates, led to a plausible mechanistic scenario. The reaction is proposed to involve carbonyl ylides but also transient species of the ketocarbene equilibrium that undergo a cascade of cycloaddition and skeletal rearrangements. [ABSTRACT FROM AUTHOR]
- Subjects :
- *DIMERIZATION
*BRONSTED acids
*CATALYSIS
*LEWIS acids
*FUNCTIONAL groups
Subjects
Details
- Language :
- English
- ISSN :
- 09476539
- Volume :
- 26
- Issue :
- 49
- Database :
- Academic Search Index
- Journal :
- Chemistry - A European Journal
- Publication Type :
- Academic Journal
- Accession number :
- 145430232
- Full Text :
- https://doi.org/10.1002/chem.202001548