Chemoselective tandem SN2′/SN2′′/inter- or intramolecular Diels–Alder reaction of γ-vinyl MBH carbonates with phenols and o-hydroxychalcones-Reference-Cited by-同舟云学术

Chemoselective tandem S_N2′/S_N2′′/inter- or intramolecular Diels–Alder reaction of γ-vinyl MBH carbonates with phenols and o-hydroxychalcones

Published:2022 Issue:70 Volume:58 Page:9794-9797
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Liu Wei¹,Zhang Le¹,Liu Ye¹,Fan Shi-Lu¹^ORCID,Dai Jian-Jun¹^ORCID,Tao Wei¹,Zhu Hui-Xia¹,Xiao Hua¹²^ORCID

Affiliation:

1. School of Food and Biological Engineering, Hefei University of Technology, 485 Danxia Road, Hefei, 230601, P. R. China

2. Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai, 200032, P. R. China

Abstract

Base-promoted chemoselective tandem SN2′/SN2′′/D–A dimerization/elimination reaction or SN2′/SN2′′/intramolecular D–A reaction of γ-vinyl Morita–Baylis–Hillman carbonates with phenols and ortho-hydroxychalcones is reported.

Funder

National Natural Science Foundation of China

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/D2CC03771H

Reference30 articles.

1. Morita–Baylis–Hillman adduct derivatives (MBHADs): versatile reactivity in Lewis base-promoted annulation

2. Transformations of Modified Morita‐Baylis‐Hillman Adducts from Isatins Catalyzed by Lewis Bases

3. Synthesis of heterocyclic compounds through nucleophilic phosphine catalysis

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