One-Pot Approach to the Conversion of Alcohols into α-Iodo-α,β-unsaturated Esters
Author:
Affiliation:
1. a Chemistry Department , College of Science, King Saud University , Riyadh, Saudi Arabia
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910903434570
Reference14 articles.
1. The Wittig and Related Reactions in Natural Product Synthesis
2. In Situ Manganese Dioxide Alcohol Oxidation−Wittig Reactions: Preparation of Bifunctional Dienyl Building Blocks
3. A Facile One‐Pot Synthesis of α‐Iodo‐α,β‐unsaturated Esters
4. The Preparation and Reactions of Some Halophosphoranes1
5. Reaction of Phosphorus Compounds. V. Resonance-stabilized α-Halomethylenephosphoranes
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1. One-Pot O2-Oxidation and the Horner–Wadsworth–Emmons Reaction of Primary Alcohols for the Synthesis of (Z)-α,β-Unsaturated Esters;The Journal of Organic Chemistry;2022-07-13
2. Tandem-, Domino- and One-Pot Reactions Involving Wittig- and Horner-Wadsworth-Emmons Olefination;Alkenes;2018-02-07
3. A facile one-pot synthesis of (Z)-α-chloro-α,β-unsaturated esters from alcohols;Arabian Journal of Chemistry;2017-05
4. Tandem oxidation–Wittig reaction using nanocrystalline barium manganate (BaMnO4); an improved one-pot protocol;Tetrahedron Letters;2016-08
5. Iodo Meyer–Schuster Rearrangement of 3-Alkoxy-2-yn-1-ols for β-Mono (Exclusively Z-Selective)-/Disubstituted α-Iodo-α,β-Unsaturated Esters;Organic Letters;2014-09-26
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