Organocatalytic Regio- and Enantioselective [3 + 2]-Annulations of Ninhydrin-Derived Morita–Baylis–Hillman Carbonates with 3-Methyleneoxindoles-Reference-Cited by-同舟云学术

Organocatalytic Regio- and Enantioselective [3 + 2]-Annulations of Ninhydrin-Derived Morita–Baylis–Hillman Carbonates with 3-Methyleneoxindoles

Published:2022-02-08 Issue:5 Volume:87 Page:3184-3194
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lu Zhongyue¹,Jia Yanwen¹,Chen Xuling¹,Li Pengfei¹²^ORCID

Affiliation:

1. Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, College of Science, Southern University of Science and Technology, Shenzhen 518055, China.

2. Key Lab of Functional Molecular Engineering of Guangdong Province, South China University of Technology, Guangzhou 510006, China

Funder

National Natural Science Foundation of China

Open Fund of the Key Laboratory of Functional Molecular Engineering of Guangdong Province

Guangdong Provincial Key Laboratory of Catalysis

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02917

Reference75 articles.

1. Synthesis of enantiomerically enriched Baylis–Hillman alcohols from their acetates: combination of kinetic resolution during the salt formation with (DHQD)2PHAL and following asymmetric induction during hydrolysis with NaHCO3 as a water surrogate

2. Alkaloids-catalyzed regio- and enantioselective allylic nucleophilic substitution of tert-butyl carbonate of the Morita–Baylis–Hillman products

3. Organocatalytic asymmetric transformations of modified Morita–Baylis–Hillman adducts

4. Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs

5. Recent Advances in Organocatalytic Asymmetric Morita–Baylis–Hillman/aza-Morita–Baylis–Hillman Reactions

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