The Baylis-Hillman reaction: An expedient synthesis of (Z)-keto allyl bromides and chlorides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydes
2. The Baylis-Hillman reaction: A novel carbon-carbon bond forming reaction
3. ?-Methylidene- and ?-Alkylidene-?-lactams from Nonproteinogenic Amino Acids
4. Hydroxyalkylation de la methylvinylcetone et de l'acrylonitrile en presence de diaza-1,4 bicyclo [2.2.2] octane
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1. Facile synthesis of biarylmethanes and tetrasubstituted arenes via a base-mediated [3 + 3] benzannulation reaction of Morita–Baylis–Hillman adducts and unsaturated sulfones;Organic & Biomolecular Chemistry;2019
2. Baylis-Hillman acetates in organic synthesis: A simple two-step strategy for oxindole-spiro-α-arylidene-γ-butyrolactone framework;Tetrahedron;2018-05
3. Halogenation of Alcohols;Comprehensive Organic Transformations;2018-02-28
4. The Baylis–Hillman reaction: a new continent in organic chemistry – our philosophy, vision and over three decades of research;New Journal of Chemistry;2018
5. Baylis-Hillman Reaction: In Situ Generated Isoquinolinium Species as Excellent Electrophiles for Coupling with Alkyl Acrylates and Acrylonitrile;European Journal of Organic Chemistry;2017-09-14
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