A Bioinspired Strategy for the Enantioselective Synthesis of Bicyclic Oxygen Heterocycles.

Biological Products / chemical synthesis Biomimetics Molecular Conformation Oxygen Isotopes Pyrans / chemical synthesis Staining and Labeling Stereoisomerism

Journal

Organic letters

ISSN: 1523-7052

Titre abrégé: Org Lett

Pays: United States

ID NLM: 100890393

Informations de publication

Date de publication:
03 04 2020

Historique:

pubmed: 17 3 2020

medline: 30 6 2021

entrez: 17 3 2020

Statut: ppublish

Résumé

A new strategy is described for the direct conversion of unsaturated 3,5-dihydroxy-diarylheptanoids to dimeric products assembled on

Identifiants

DOI: 10.1021/acs.orglett.0c00425 PMID: 32176515

pubmed: 32176515

doi: 10.1021/acs.orglett.0c00425

doi:

Substances chimiques

Biological Products 0

Oxygen Isotopes 0

Oxygen-18 0

Pyrans 0

blepharocalyxin D 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

Pagination

2548-2552

A Bioinspired Strategy for the Enantioselective Synthesis of Bicyclic Oxygen Heterocycles.

Journal

Informations de publication

Résumé

Identifiants

Substances chimiques

Types de publication

Langues

Sous-ensembles de citation

Pagination

Auteurs

Edith Rodriguez Venegas (ER)

Christine L Willis (CL)

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Classifications MeSH