Aziridination of alkenes using 3-acetoxyaminoquinazolin-4(3H)ones: nucleophilic attack by the acetoxyamino group on ester-substituted allylic alcohols-Reference-Cited by-同舟云学术

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Aziridination of alkenes using 3-acetoxyaminoquinazolin-4(3H)ones: nucleophilic attack by the acetoxyamino group on ester-substituted allylic alcohols

Published:1994 Issue:18 Volume: Page:2031
ISSN:0022-4936
Container-title:Journal of the Chemical Society, Chemical Communications
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Atkinson Robert S.,Fawcett John,Russell David R.,Williams Paul J.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940002031

Cited by 31 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. Strategies for Direct, Transition Metal‐Free Addition of Nitrogen Synthons to Alkenes;Helvetica Chimica Acta;2023-12-15

2. Novel Synergistic Catalysis by Ethylcarbodiimide Hydrochloride Salt and CuI Towards Morita‐Baylis‐Hillman Reaction;ChemistrySelect;2023-02-02

3. Transformations of Functional Groups in Morita–Baylis–Hillman Adducts;The Chemistry of the Morita-Baylis-Hillman Reaction;2011-04-04

4. Recent Contributions from the Baylis−Hillman Reaction to Organic Chemistry;Chemical Reviews;2010-08-24

5. ChemInform Abstract: Aziridination of Alkenes Using 3-Acetoxyaminoquinazolin-4(3H)ones: Nucleophilic Attack by the Acetoxyamino Group on Ester-Substituted Allylic Alcohols.;ChemInform;2010-08-18

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