A Catalytic Approach for Enantioselective Synthesis of Homoallylic Alcohols Bearing a Z-Alkenyl Chloride or Trifluoromethyl Group. A Concise and Protecting Group-Free Synthesis of Mycothiazole-Reference-Cited by-同舟云学术

A Catalytic Approach for Enantioselective Synthesis of Homoallylic Alcohols Bearing a Z-Alkenyl Chloride or Trifluoromethyl Group. A Concise and Protecting Group-Free Synthesis of Mycothiazole

Published:2019-12-24 Issue:1 Volume:142 Page:436-447
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Morrison Ryan J.¹,van der Mei Farid W.¹,Romiti Filippo¹²^ORCID,Hoveyda Amir H.¹²^ORCID

Affiliation:

1. Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, United States

2. Supramolecular Science and Engineering Institute, University of Strasbourg, CNRS, Strasbourg 67000, France

Funder

Centre National de la Recherche Scientifique

National Institutes of Health

Frontiers in Chemistry Research Fondation, University of Strasbourg

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b11178

Reference75 articles.

1. Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones

2. Catalytic Enantioselective Allylation of Carbonyl Compounds and Imines

3. The macrolactins, a novel class of antiviral and cytotoxic macrolides from a deep-sea marine bacterium

4. Total Synthesis of (−)-Macrolactin A

5. Total Synthesis of Macrolactin A with Versatile Catalytic, Enantioselective Dienolate Aldol Addition Reactions

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