Radical-based methodology for efficient generation of acyclic N-acylimines

W. Chao; S. M. Weinreb

doi:10.1016/S0040-4039(00)01683-X

Radical-based methodology for efficient generation of acyclic N-acylimines

W. Chao
, S. M. Weinreb

Chemistry

Research output: Contribution to journal › Article › peer-review

28 Scopus citations

Abstract

α-Methoxybenzamides 11, which are convenient precursors of acyclic N-acylimines, can be cleanly generated in high yields via a free radical process starting from an o-aminobenzamide 16 derived from an N-t-butyl or N-cumyl secondary amine. (C) 2000 Elsevier Science Ltd.

Original language	English (US)
Pages (from-to)	9199-9204
Number of pages	6
Journal	Tetrahedron Letters
Volume	41
Issue number	48
DOIs	https://doi.org/10.1016/S0040-4039(00)01683-X
State	Published - Nov 25 2000

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)01683-X

Cite this

@article{cf347da52b59481e9fca19c994ba812d,

title = "Radical-based methodology for efficient generation of acyclic N-acylimines",

abstract = "α-Methoxybenzamides 11, which are convenient precursors of acyclic N-acylimines, can be cleanly generated in high yields via a free radical process starting from an o-aminobenzamide 16 derived from an N-t-butyl or N-cumyl secondary amine. (C) 2000 Elsevier Science Ltd.",

author = "W. Chao and Weinreb, \{S. M.\}",

note = "Funding Information: We are grateful to the National Institutes of Health (CA-32299) for financial support of this research.",

year = "2000",

month = nov,

day = "25",

doi = "10.1016/S0040-4039(00)01683-X",

language = "English (US)",

volume = "41",

pages = "9199--9204",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "48",

}

TY - JOUR

T1 - Radical-based methodology for efficient generation of acyclic N-acylimines

AU - Chao, W.

AU - Weinreb, S. M.

N1 - Funding Information: We are grateful to the National Institutes of Health (CA-32299) for financial support of this research.

PY - 2000/11/25

Y1 - 2000/11/25

N2 - α-Methoxybenzamides 11, which are convenient precursors of acyclic N-acylimines, can be cleanly generated in high yields via a free radical process starting from an o-aminobenzamide 16 derived from an N-t-butyl or N-cumyl secondary amine. (C) 2000 Elsevier Science Ltd.

AB - α-Methoxybenzamides 11, which are convenient precursors of acyclic N-acylimines, can be cleanly generated in high yields via a free radical process starting from an o-aminobenzamide 16 derived from an N-t-butyl or N-cumyl secondary amine. (C) 2000 Elsevier Science Ltd.

UR - https://www.scopus.com/pages/publications/0034715997

UR - https://www.scopus.com/pages/publications/0034715997#tab=citedBy

U2 - 10.1016/S0040-4039(00)01683-X

DO - 10.1016/S0040-4039(00)01683-X

M3 - Article

AN - SCOPUS:0034715997

SN - 0040-4039

VL - 41

SP - 9199

EP - 9204

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 48

ER -

Radical-based methodology for efficient generation of acyclic N-acylimines

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this