An improved synthesis of a ring-C precursor to cobyric acid

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Abstract

Alkyne acid 10 was prepared in enantioselective fashion from allylic ester derivative (R)-18 via an E-selective Ireland-Claisen rearrangement followed by Si-assisted elimination of HBr. The present route offers significant advantages in terms of both scalability and overall yield compared to that previously described. Alkyne acid 10 is an attractive ring-C precursor for an ongoing synthesis of cobyric acid. © ARKAT USA, Inc.

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APA

Wang, H., & Jacobi, P. A. (2010). An improved synthesis of a ring-C precursor to cobyric acid. Arkivoc, 2010(4), 15–24. https://doi.org/10.3998/ark.5550190.0011.403

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