Studies toward the total synthesis of (+)‐neopeltolide using <scp> <i>N</i> </scp> ‐heterocyclic carbene‐catalyzed oxo‐acyloxylation/reductive oxa‐Michael addition strategy-Reference-Cited by-同舟云学术

Studies toward the total synthesis of (+)‐neopeltolide using N ‐heterocyclic carbene‐catalyzed oxo‐acyloxylation/reductive oxa‐Michael addition strategy

Published:2022-08-18 Issue:10 Volume:43 Page:1169-1172
ISSN:1229-5949
Container-title:Bulletin of the Korean Chemical Society
language:en
Short-container-title:Bulletin Korean Chem Soc

Author:

Reddi Rambabu N.¹,Sudalai Arumugam¹,Jo Changbum²^ORCID

Affiliation:

1. Chemical Engineering and Process Development Division CSIR‐National Chemical Laboratory Pune Maharashtra India

2. Department of Chemistry and Chemical Engineering Inha University Michuhol‐gu, Incheon Republic of Korea

Funder

Inha University

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bkcs.12604

Reference43 articles.

1. The exploration of macrocycles for drug discovery — an underexploited structural class

2. Macrocyclic Inhibitors of Hsp90

3. Macrocycles Are Great Cycles: Applications, Opportunities, and Challenges of Synthetic Macrocycles in Drug Discovery

4. Biologically Active Macrocyclic Compounds – from Natural Products to Diversity‐Oriented Synthesis

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

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1. Total Synthesis of Marine Macrolide Natural Products by the Macrocyclization/Transannular Pyran Cyclization Strategy;Synlett;2023-09-26

2. An 11-Step Synthesis of (+)-Neopeltolide by the Macrocyclization/Transannular Pyran Cyclization Strategy;Bulletin of the Chemical Society of Japan;2023-02-03