Convergent Total Synthesis of Paecilomycin B and 6′-epi-Paecilomycin B by a Barbier-Type Reaction Using 2,4,6-Triisopropylphenyllithium-Reference-Cited by-同舟云学术

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Convergent Total Synthesis of Paecilomycin B and 6′-epi-Paecilomycin B by a Barbier-Type Reaction Using 2,4,6-Triisopropylphenyllithium

Published:2018-02-08 Issue:13 Volume:83 Page:7019-7032
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ohba Kiyomi¹^ORCID,Nakata Masaya²

Affiliation:

1. Research Unit, Innovative Medical Science, Mitsubishi Tanabe Pharma Corporation, 1000 Kamoshida-cho, Aoba-ku, Yokohama 227-0033, Japan

2. Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b03041

Reference62 articles.

1. Recent progress regarding the bioactivities, biosynthesis and synthesis of naturally occurring resorcinolic macrolides

2. Benzenediol lactones: a class of fungal metabolites with diverse structural features and biological activities

3. New Efficient Synthesis of Resorcinylic Macrolides via Ynolides: Establishment of Cycloproparadicicol as Synthetically Feasible Preclinical Anticancer Agent Based on Hsp90 as the Target

4. Total synthesis of LL-Z1640-2 utilizing a late-stage intramolecular Nozaki–Hiyama–Kishi reaction

5. Chemical syntheses of the cochliomycins and certain related resorcylic acid lactones

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