Highly regioselective hydroiodination of terminal alkynes and silylalkynes with iodine and phosphorus reagents leading to internal iodoalkenes-Reference-Cited by-同舟云学术

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Highly regioselective hydroiodination of terminal alkynes and silylalkynes with iodine and phosphorus reagents leading to internal iodoalkenes

Published:2012-11 Issue:47 Volume:68 Page:9818-9825
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kawaguchi Shin-ichi,Masuno Haruna,Sonoda Motohiro,Nomoto Akihiro,Ogawa Akiya

Funder

Ministry of Education, Culture, Sports, Science and Technology, Japan

Industry-University Cooperation Program of Sakai City

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference74 articles.

1. Iodoalkenes were widely used as intermediates for organic synthesis. For examples, see:

2. For recently examples, see:

3. Stereocontrolled total synthesis of (+)-concanamycin F: the strategic use of boron-mediated aldol reactions of chiral ketones

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1. Mn(II)-Catalyzed Markovnikov Hydroiodination of Terminal Aryl Alkynes;The Journal of Organic Chemistry;2024-07-27

2. Recent Progress in Haloalkene Synthesis by Hydrohalogenation (HX=HCl, HBr, HI) of Alkynes;Advanced Synthesis & Catalysis;2024-04-05

3. Regio- and Stereocontrolled Hydrohalogenation of Ynamides with N-Halosuccinimides (NXS) as the Halogen Source: Synthesis of (E)-α-Haloenamides;The Journal of Organic Chemistry;2024-01-18

4. Hydrohalogenation of Electron-Deficient Alkyne in Aqueous Solution;Hans Journal of Chemical Engineering and Technology;2024

5. Rhodium‐katalysierte Anti‐Markovnikov Hydroiodierung von Terminalen Alkinen**;Angewandte Chemie;2022-12-20

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