Bioinspired enantioselective total syntheses of antibacterial callistrilones enabled by double S<sub>N</sub>2′ cascade-Reference-Cited by-同舟云学术

Bioinspired enantioselective total syntheses of antibacterial callistrilones enabled by double S_N2′ cascade

Published:2022 Issue:36 Volume:58 Page:5474-5477
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Dethe Dattatraya H.¹^ORCID,Dherange Balu D.¹^ORCID,Das Saikat¹,Srivastava Aparna¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, 208016, India

Abstract

A bioinspired, enantioselective total syntheses of antibacterial callistrilones A, C–E and 13-epi-callistrilone E with an unprecedented, sterically compact [1]benzofuro-[2,3-a]xanthene 6/6/6/5/6/3-fused hexacyclic skeleton is described.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D2CC01398C

Reference26 articles.

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2. Syntheses of (+)-30-epi-, (−)-6-epi-, (±)-6,30-epi-13,14-Didehydroxyisogarcinol and (±)-6,30-epi-Garcimultiflorone A Utilizing Highly Diastereoselective, Lewis Acid-Controlled Cyclizations

3. Polycyclic Polyprenylated Acylphloroglucinols

4. Biomimetic Total Synthesis of Hyperjapones A–E and Hyperjaponols A and C

5. Guajavadimer A, a Dimeric Caryophyllene-Derived Meroterpenoid with a New Carbon Skeleton from the Leaves of Psidium guajava

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