The use of acetylenic aldehydes in Baylis–Hillman reactions: synthesis of versatile allyl propargyl alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Evidence of single electron transfer in the reduction of various organic substrates by lithium tetra(N-dihydropyridyl)aluminate
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3. Recent topics in the chemistry of synthetic pyrethroids containing certain secondary alcohol moieties
4. Stereo- and Enantioselective Synthesis of Bothcis-Chrysanthemic Acid Methyl Esters in High Optical Purity
5. Preparative bioorganic chemistry. Part III. Preparation of optically active secondary alcohols related to synthetic pyrethroids by microbial asymmetric hydrolysis of the corresponding acetates.
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1. A Facile Approach to 3,4‐Oxepino‐Fused Tricyclic Indoles from MBH‐Acetates of Acetylenic AldehydesviaSuccessive Allylic Substitution/Intramolecular [3+2] Annulation†;ChemistrySelect;2019-07-25
2. Alkylation and Acylation of Aldehydes, Ketones, and Their Derivatives;Comprehensive Organic Transformations;2018-02-28
3. SYNTHESIS OF a -ACETYLENIC ALDEHYDES;Bashkir chemistry journal;2018-02
4. Total synthesis of distaminolyne A;Tetrahedron Letters;2017-03
5. A facile one-pot synthesis of novel 1-substituted 2-(8-hydroxyquinolin-5-yl)-1,5,6,7-tetrahydro-6,6-dimethyl- 4H-indol-4-one derivatives;Arkivoc;2016-06-07
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