A simple method for the conversion of propargyl alcohols to symmetrical 1,5-diynes using low valent titanium reagents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. First synthesis of cis-enediynes from 1,5-diynes by an acid-mediated allylic rearrangement
2. Synthesis ofcis-Enediynes from 1,5-Diynes by Rearrangement of an Allylic Double Bond
3. A Direct and Stereocontrolled Route to Conjugated Enediynes
4. Highly efficient photochemical synthesis of the enediyne functionality via a Norrish type II reaction
5. Selective carbon-carbon bond formation via transition metal catalysis. 23. Highly selective and convenient method for the synthesis of 1,5-enynes and 1,5-dienes by the reaction of 1,3-dilithiopropargyl phenyl sulfide with allylic halides
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1. Photoredox Selective Homocoupling of Propargyl Bromides;The Journal of Organic Chemistry;2022-11-01
2. NHC and visible light-mediated photoredox co-catalyzed 1,4-sulfonylacylation of 1,3-enynes for tetrasubstituted allenyl ketones;Chemical Science;2022
3. Mechanistic Features of the Oxidation–Reductive Coupling of Alcohols Catalyzed by Oxo-Vanadium Complexes;Inorganic Chemistry;2018-12-07
4. Low-Valent Titanium-Mediated Radical Conjugate Addition Using Benzyl Alcohols as Benzyl Radical Sources;Organic Letters;2018-08-27
5. Mechanistic Insights into the ReIO2(PPh3)2-Promoted Reductive Coupling of Alcohols;Organometallics;2018-07-19
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