Highly diastereoselective annulation of 2-substituted 3-nitro-2<i>H</i>-chromenes with hemicurcuminoids and curcuminoids <i>via</i> a double and triple Michael reaction cascade-Reference-Cited by-同舟云学术

Highly diastereoselective annulation of 2-substituted 3-nitro-2H-chromenes with hemicurcuminoids and curcuminoids via a double and triple Michael reaction cascade

Published:2022 Issue:33 Volume:46 Page:16047-16057
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Zimnitskiy Nikolay S.¹^ORCID,Barkov Alexey Yu.¹^ORCID,Kochnev Ivan A.¹,Kutyashev Igor B.¹^ORCID,Korotaev Vladislav Yu.¹^ORCID,Sosnovskikh Vyacheslav Ya.¹^ORCID

Affiliation:

1. Institute of Natural Sciences and Mathematics, Ural Federal University, 620000, Ekaterinburg, Russian Federation

Abstract

One-pot stereoselective methods for the synthesis of hexahydro-9H-benzo[c]chromen-9-ones and hexahydro-1H,6H-chromeno[6,5-c]chromen-1-ones have been developed.

Funder

Russian Foundation for Basic Research

Ministry of Science and Higher Education of the Russian Federation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ02019J

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1. Natural Product-like Combinatorial Libraries Based on Privileged Structures. 1. General Principles and Solid-Phase Synthesis of Benzopyrans

2. Diversity-oriented synthesis: producing chemical tools for dissecting biology