Formal Halo‐Meyer–Schuster Rearrangement of Propargylic Acetates through a Novel Intermediate and an Unexampled Mechanistic Pathway-Reference-Cited by-同舟云学术

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Formal Halo‐Meyer–Schuster Rearrangement of Propargylic Acetates through a Novel Intermediate and an Unexampled Mechanistic Pathway

Published:2019-07-04 Issue:42 Volume:25 Page:9816-9820
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Sadhukhan Santu¹,Baire Beeraiah¹^ORCID

Affiliation:

1. Department of ChemistryIndian Institute of Technology Madras Chennai Tamilnadu 600036 India

Funder

Science and Engineering Research Board

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201901856

Reference68 articles.

1.

2. FeCl3-Catalyzed Nucleophilic Substitution of Propargylic Acetates with Enoxysilanes

3. Carbocyclisation of alkynes with external nucleophiles catalysed by gold, platinum and other electrophilic metals

4. Rhodium-catalyzed acyloxy migration of propargylic esters in cycloadditions, inspiration from the recent “gold rush”

5. Recent Advances on the Lewis Acid-Catalyzed Cascade Rearrangements of Propargylic Alcohols and Their Derivatives

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