NEW SYNTHESIS OF SECONDARY CARBOXAMIDE BY USING 2-METHYL-2-OXAZILONE AS A BUILDING BLOCK

DOI: 10.1016/S0040-4039(00)98160-7

Source and publish data:

Tetrahedron Letters p. 3235 - 3238 (1985)

Update date:2022-08-04

Topics:

Authors:

Inaba, Masami

Moriwake, Toshio

Saito, Seiki

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(00)98160-7

New method for the synthesis of secondary carboxamides of type, R²NHCOR¹, which utilizes 2-methyl-2-oxazoline as a carboxamide building block and various halides, R²X, has been developed.

Full text of DOI:10.1016/S0040-4039(00)98160-7

Products guided by the article

Product name:N-(2-Phenylselanyl-ethyl)-N-prop-2-ynyl-acetamide

Cas No:99306-98-6

R&D Labs maybe for 99306-98-6

Nanjing lanbai chemical Co.,Ltd.

Contact:+86-25-85499326

Address:Room 908, 9F Taiyue Building,No.285 Heyan Road
xujianqiang

Contact:86-21-57725962

Address:shanghai
Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
JinTan Pingsheng Chemical Co.,Ltd

Contact:+86-519-82828200

Address:NO.11Danfengxilu Road,Jintan City,Jiangsu,China
NANCHANG QINZHI SCI&TEC.CO.,LTD(expird)

Contact:+86-13687004106

Address:Hero South Road,Hero Zone,Nanchang,Jiangxi,China

Relevant to this article

Total synthesis of two natural phenanthrenes: confusarin and a regioisomer

Doi:10.1016/j.tet.2007.09.052
(2007)
Indium(III) bromide catalyzed rapid propargylation of heteroaromatic systems by α-aryl-substituted propargyl alcohols

Doi:10.1055/s-2007-990797
(2007)
Synthesis of one-dimensional metal-containing insulated molecular wire with versatile properties directed toward molecular electronics materials

Doi:10.1021/ja411665k
(2014)
Design, structure-activity relationship, and pharmacokinetic profile of pyrazole-based indoline factor Xa inhibitors

Doi:10.1016/j.bmcl.2007.09.091
(2007)
Catalytic asymmetric nitro-Mannich reactions with a Yb/K heterobimetallic catalyst

Doi:10.3390/molecules15031280
(2010)
Doi:10.1021/jo01083a619
(1959)

Article Doi