Highly efficient triphenyl(3-sulfopropyl)phosphonium functionalized phosphotungstic acid on silica as a solid acid catalyst for selective mono-allylation of acetals-Reference-Cited by-同舟云学术

Highly efficient triphenyl(3-sulfopropyl)phosphonium functionalized phosphotungstic acid on silica as a solid acid catalyst for selective mono-allylation of acetals

Published:2015 Issue:8 Volume:5 Page:4039-4047
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Kamble Sumit B.¹²³⁴,Shinde Suhas H.¹²³⁴,Rode Chandrashekhar V.¹²³⁴

Affiliation:

1. Chemical Engineering & Process Development Division

2. CSIR-National Chemical Laboratory

3. Pune 411008

4. India

Abstract

A silica-supported zwitterion-functionalized phosphotungstic acid catalyst developed for the selective Hosomi–Sakurai reaction giving 93–99% yield of homoallyl ethers.

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CY/C5CY00531K

Reference56 articles.

1. Sakurai Reaction of 3,3-Bis(silyl) Silyl Enol Ethers with Acetals Involving Selective Desilylation of the Geminal Bis(silane). Concise Synthesis of Nematocidal Oxylipid

2. Total Synthesis of Natural Enantiomers of Heliespirones A and C via the Diastereoselective Intramolecular Hosomi-Sakurai Reaction

3. Iron-catalyzed N-alkylation using π-activated ethers as electrophiles

4. Iridium-Catalyzed (Z)-Trialkylsilylation of Terminal Olefins

5. Palladium-Catalyzed Allylic Acyloxylation of Terminal Alkenes in the Presence of a Base

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