Highly chemoselective rearrangement of 3-aryloxaziridines to nitrones or amides

Dong Xing; Xinfang Xu; Liping Yang

doi:10.1055/s-0029-1216965

Highly chemoselective rearrangement of 3-aryloxaziridines to nitrones or amides

Dong Xing
, Xinfang Xu
, Liping Yang^*

^*此作品的通讯作者

化学与分子工程学院

East China Normal University

科研成果: 期刊稿件 › 文章 › 同行评审

13 引用（Scopus）

摘要

An efficient method for the chemoselective ring-opening rearrangement of 3-aryloxaziridines by using silver triflate alone to afford nitrones, or in the presence of a simple Br0nsted acid to yield amides, has been developed. Silver triflate plays an important role in both transformations.

源语言	英语
页（从-至）	3399-3404
页数	6
期刊	Synthesis (Germany)
期	20
DOI	https://doi.org/10.1055/s-0029-1216965
出版状态	已出版 - 2009

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10.1055/s-0029-1216965

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@article{bc37eee1eb42450cbc0fe23723f7efeb,

title = "Highly chemoselective rearrangement of 3-aryloxaziridines to nitrones or amides",

abstract = "An efficient method for the chemoselective ring-opening rearrangement of 3-aryloxaziridines by using silver triflate alone to afford nitrones, or in the presence of a simple Br0nsted acid to yield amides, has been developed. Silver triflate plays an important role in both transformations.",

keywords = "Amides, Chemoselectivity, Nitrones, Oxaziridines, Rearrangement",

author = "Dong Xing and Xinfang Xu and Liping Yang",

year = "2009",

doi = "10.1055/s-0029-1216965",

language = "英语",

pages = "3399--3404",

journal = "Synthesis (Germany)",

issn = "0039-7881",

publisher = "Georg Thieme Verlag",

number = "20",

}

TY - JOUR

T1 - Highly chemoselective rearrangement of 3-aryloxaziridines to nitrones or amides

AU - Xing, Dong

AU - Xu, Xinfang

AU - Yang, Liping

PY - 2009

Y1 - 2009

N2 - An efficient method for the chemoselective ring-opening rearrangement of 3-aryloxaziridines by using silver triflate alone to afford nitrones, or in the presence of a simple Br0nsted acid to yield amides, has been developed. Silver triflate plays an important role in both transformations.

AB - An efficient method for the chemoselective ring-opening rearrangement of 3-aryloxaziridines by using silver triflate alone to afford nitrones, or in the presence of a simple Br0nsted acid to yield amides, has been developed. Silver triflate plays an important role in both transformations.

KW - Amides

KW - Chemoselectivity

KW - Nitrones

KW - Oxaziridines

KW - Rearrangement

UR - https://www.scopus.com/pages/publications/72049125871

U2 - 10.1055/s-0029-1216965

DO - 10.1055/s-0029-1216965

M3 - 文章

AN - SCOPUS:72049125871

SN - 0039-7881

SP - 3399

EP - 3404

JO - Synthesis (Germany)

JF - Synthesis (Germany)

IS - 20

ER -

Highly chemoselective rearrangement of 3-aryloxaziridines to nitrones or amides

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