Phosphonic Acids and Esters. XVII. Formation, Aromatization, and Reduction of Diels—Alder Adducts of Vinyl- and Chlorovinylphosphonates1
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo01348a033
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1. Catalyst-free Diels–Alder reactions of vinylphosphonates with cyclopentadienones;Canadian Journal of Chemistry;2017-08
2. Utility of Bifunctional N-Heterocyclic Phosphine (NHP)-Thioureas for Metal-Free Carbon–Phosphorus Bond Construction toward Regio- and Stereoselective Formation of Vinylphosphonates;The Journal of Organic Chemistry;2015-12-15
3. Phosphonated homopolymers and copolymers via ring opening metathesis polymerization: T g tuning, flame resistance, and photolithography;Journal of Polymer Science Part A: Polymer Chemistry;2015-12-02
4. Tetraethyl Vinylidenebisphosphonate: A Versatile Synthon for the Preparation of Bisphosphonates;Synthesis;2014-03-19
5. Properties and Reactions of Phosphonic and Phosphinic Acids and their Derivatives;PATAI'S Chemistry of Functional Groups;2009-12-15
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