Document Type
Article
Publication Date
2010
Publication Title
ARKIVOC - Online Journal of Organic Chemistry
Department
Department of Chemistry
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.
Dartmouth Digital Commons Citation
Wang, Hui and Jacobi, Peter A., "An Improved Synthesis of a Ring-C Precursor to Cobyric Acid" (2010). Dartmouth Scholarship. 505.
https://digitalcommons.dartmouth.edu/facoa/505
