Vinylogous and stereoselective domino synthesis of pyrano[2,3- c]pyrroles from alkylidene meldrum's acids
- PMID: 38482880
- DOI: 10.1039/d4ob00233d
Vinylogous and stereoselective domino synthesis of pyrano[2,3- c]pyrroles from alkylidene meldrum's acids
Abstract
A domino Vinylogous aza-Michael-Aldol-Cyclocondensation (aza-VMAC) reaction was achieved with a series of alkylidene Meldrum's acid derivatives under simple operational conditions paving the way to novel pyrano[2,3-c]pyrroles in an excellent diasteroselectivity (>96 : 4), encompassing the relative control of three contiguous stereocenters.
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