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• W2018396340 abstract "An enantioselective formal synthesis of (−)-englerin A (1) is reported. Key to the strategy is a Rh-catalyzed [4 + 3] cycloaddition reaction between furan 10 and diazo ester 11 that, following an intramolecular aldol condensation, produces the tricyclic scaffold of englerin. This strategy also provides a rapid, efficient, and stereoselective access to the biologically significant core motif of the guaiane sesquiterpenes." @default.
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• W2018396340 date "2010-07-29" @default.
• W2018396340 modified "2023-09-27" @default.
• W2018396340 title "Enantioselective Formal Synthesis of (−)-Englerin A via a Rh-Catalyzed [4 + 3] Cycloaddition Reaction" @default.
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• W2018396340 doi "https://doi.org/10.1021/ol1015652" @default.
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