Synthesis of Highly Substituted Aminotetrahydropyrans Enabled by Stereospecific Multivector C–H Functionalization-Reference-Cited by-同舟云学术

Synthesis of Highly Substituted Aminotetrahydropyrans Enabled by Stereospecific Multivector C–H Functionalization

Published:2023-06-09 Issue: Volume: Page:
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kang Guowei¹^ORCID,Xiao Li-Jun¹^ORCID,Hesp Kevin D.²^ORCID,Huh Chan Woo³,Lian Yajing³,Richardson Paul⁴^ORCID,Schmitt Daniel C.³^ORCID,Hong Kai¹^ORCID,Yu Jin-Quan¹^ORCID

Affiliation:

1. Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

2. Treeline Biosciences, 500 Arsenal St, second Floor, Watertown, Massachusetts 02472, United States

3. Medicine Design, Pfizer Inc., Groton, Connecticut 06340, United States

4. Medicine Design, Pfizer Inc., San Diego, California 92121, United States

Funder

Pfizer

Scripps Research Institute

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01439

Reference22 articles.

1. Diarylheptanoids of Centrolobium species

2. Neopeltolide, a Macrolide from a Lithistid Sponge of the Family Neopeltidae

3. New Cytotoxic 14-Membered Macrolides from Marine-Derived Fungus Aspergillus ostianus

4. Strategies for the Formation of Tetrahydropyran Rings in the Synthesis of Natural Products

5. Strategies for the construction of tetrahydropyran rings in the synthesis of natural products

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