A DFT study of the <i>endo</i>-selectivity mechanism of the Diels–Alder reaction in lindenane dimeric sesquiterpene synthesis promoted by pyridines-Reference-Cited by-同舟云学术

A DFT study of the endo-selectivity mechanism of the Diels–Alder reaction in lindenane dimeric sesquiterpene synthesis promoted by pyridines

Published:2023 Issue:5 Volume:25 Page:3772-3779
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Li Yuxin¹^ORCID,Zhang Rong¹,Song Yuling²,Xie Hujun²^ORCID,Wu Ruibo¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, People's Republic of China

2. School of Food Science and Biotechnology, Zhejiang Gongshang University, Hangzhou 310018, People's Republic of China

Abstract

DFT calculation revealed that that hydrogen bond interaction plays an important role in the endo-selectivity of the Diels-Alder reaction between lindenane sesquiterpenes promoted by pyridines.

Funder

Special Project for Research and Development in Key areas of Guangdong Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CP/D2CP04986D

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3. Nine sesquiterpenoid dimers with four unprecedented types of carbon skeleton from Chloranthus henryi var. hupehensis

4. Benzyl 2-β-Glucopyranosyloxybenzoate, a New Phenolic Acid Glycoside from Sarcandra glabra

5. Sesquiterpene dimers esterified with diverse small organic acids from the seeds of Sarcandra glabra

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