Highly Diastereo‐ and Enantioselective Synthesis of 3,6′‐Bisboryl‐ anti ‐1,2‐oxaborinan‐3‐enes: An Entry to Enantioenriched Homoallylic Alcohols with A Stereodefined Trisubstituted Alkene
Author:
Affiliation:
1. Department of Chemistry and Biochemistry Auburn University Auburn AL 36849 USA
Funder
Auburn University
Publisher
Wiley
Subject
General Chemistry,Catalysis
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202006420
Reference122 articles.
1. For selected natural products that incorporate homoallylic alcohols bearing trisubstituted olefins see:
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4. Nongenetic Reprogramming of a Fungal Highly Reducing Polyketide Synthase
5. Chemoenzymatic Total Synthesis and Structural Diversification of Tylactone-Based Macrolide Antibiotics through Late-Stage Polyketide Assembly, Tailoring, and C—H Functionalization
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