A deconstruction–reconstruction strategy to access 1-naphthol derivatives: application to the synthesis of aristolactam scaffolds-Reference-Cited by-同舟云学术

A deconstruction–reconstruction strategy to access 1-naphthol derivatives: application to the synthesis of aristolactam scaffolds

Published:2023 Issue:44 Volume:21 Page:8936-8941
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Bak Jeong Min¹,Song Moonyeong²,Shin Inji²^ORCID,Lim Hee Nam¹^ORCID

Affiliation:

1. Department of Chemistry, Yeungnam University, 280 Daehak-Ro, Gyeongsan, Gyeongbuk, 38541, Republic of Korea

2. Department of Fine Chemistry, Seoul National University of Science and Technology, 232 Gongneung-ro, Nowon-gu, Seoul 01811, Republic of Korea

Abstract

A fragmentation–annulation reaction of α-oximinoindanones for the synthesis of 1-naphthol derivatives has been delineated in a highly practical manner. The utility was further demonstrated in the multi-step synthesis of a tetracyclic aristolactam analogue.

Funder

National Research Foundation of Korea

Seoul National University of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01603J

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