Base catalysed rearrangements involving ylide intermediates. Part 15. The mechanism of the Stevens [1,2] rearrangement-Reference-Cited by-同舟云学术

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Base catalysed rearrangements involving ylide intermediates. Part 15. The mechanism of the Stevens [1,2] rearrangement

Published:1983 Issue: Volume: Page:1009
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Ollis W. David,Rey Max,Sutherland Ian O.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1983/P1/P19830001009

Cited by 143 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent Advances in Asymmetric [1,2]-Stevens-Type Rearrangement via Metal Carbenes;Synthesis;2023-03-08

2. Nitrogen- and Sulfur-Based Stevens and Related Rearrangements;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

3. Oxonium Ylides Generated from 1,4‐Disubstituted α‐Diazo Glutaconimides: a Rich Source of Diverse Oxygen Heterocyclic Frameworks;European Journal of Organic Chemistry;2021-06-17

4. Perfluorobutyl Iodide Mediated [1,2] and [2,3] Stevens Rearrangement for the Synthesis of Indolin‐3‐Ones;Advanced Synthesis & Catalysis;2020-09-02

5. Copper-assisted synthesis of five-memberedO-heterocycles;Inorganic and Nano-Metal Chemistry;2020-02-13

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