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-Reference-Cited by-同舟云学术

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

Published:2020-11-10 Issue:2 Volume:133 Page:853-861
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Chen Jichao¹,Miliordos Evangelos¹,Chen Ming¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry Auburn University Auburn AL 36849 USA

Funder

Auburn University

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.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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