ZnCl2-mediated stereo- and chemoselective synthesis of vinylphosphonates
Author:
Affiliation:
1. Department of Chemistry, Institute for Advanced Studies in Basic Sciences, Gava Zang, Zanjan, Iran
2. School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan
Abstract
Funder
Institute for Advanced Studies in Basic Sciences
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB00037G
Reference38 articles.
1. Vinylphosphonates in Organic Synthesis
2. Celebrating 20 Years of SYNLETT - Special Essay: General Procedure for the Palladium-Catalyzed Selective Hydrophosphorylation of Alkynes
3. Transition-Metal-Catalyzed Addition of Heteroatom−Hydrogen Bonds to Alkynes
4. Sequential Double Olefination of 2-(Arylmethylidene)-2-phosphonoacetonitrile with Dimsyl Lithium and Aldehydes: A Domino Route to Densely Substituted 1,3-Butadienes
5. Strategies for the synthesis of α- and β-amino vinylphosphonate
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1. Preparation of Vinylphosphonates from Ketones Promoted by Tf2O;The Journal of Organic Chemistry;2023-02-21
2. Stereoselective synthesis of vinylphosphonates through aromatic aza-Claisen rearrangement of α-aminophosphonates;Chemical Communications;2023
3. Highly Stereoselective Synthesis of 2, 2‐Disubstituted Vinylphosphonates via Aryl to Vinyl 1, 4‐Palladium Migration;Chinese Journal of Chemistry;2022-07-07
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