DBU-mediated C-C bond formation between Baylis-Hillman Acetates and Active Methylene Compounds

A new reagent system for the formation of C-C bond between the Baylis-Hillman acetates and active methylene compounds (AMCs) were developed. This method provides tri-substituted alkenes as the major product in good yield under neat condition. The reaction proceeds through the SN2ꞌ mechanism to give substituted alkenes in good yields with high stereoselectivity. 1,8-diazabicyclo(5.4.0)undec-7-ene (DBU) act as a unique base which accelerate the rate of the reaction.

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Publication Details

Journal
Indian Journal of Chemistry
Published
2025-02-20
DOI
https://doi.org/10.56042/ijc.v64i2.15867
Primary Topic
Synthesis of heterocyclic compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

DBU-mediated C-C bond formation between Baylis-Hillman Acetates and Active Methylene Compounds

Indian Journal of Chemistry
Synthesis of heterocyclic compounds
article

DBU-mediated C-C bond formation between Baylis-Hillman Acetates and Active Methylene Compounds

article en

Abstract

A new reagent system for the formation of C-C bond between the Baylis-Hillman acetates and active methylene compounds (AMCs) were developed. This method provides tri-substituted alkenes as the major product in good yield under neat condition. The reaction proceeds through the SN2ꞌ mechanism to give substituted alkenes in good yields with high stereoselectivity. 1,8-diazabicyclo(5.4.0)undec-7-ene (DBU) act as a unique base which accelerate the rate of the reaction.

Indian Journal of ChemistryVol. 64(2)
North Eastern Regional Institute of Science and Technology (IN)
University Grants Commission
Openalex Percentile: Top 98%
Synthesis of heterocyclic compounds
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DBU-mediated C-C bond formation between Baylis-Hillman Acetates and Active Methylene Compounds · Indian Journal of Chemistry (2025) | TGRS Research Map | TGRS