A General Synthesis of Mono- and Disubstituted 1,4,7-Triazacyclononanes

DOI: 10.1016/0040-4039(95)02009-E

Source and publish data:

Tetrahedron Letters p. 9269 - 9272 (1995)

Update date:2022-08-03

Topics:

Authors:

Kovacs, Zoltan

Sherry, A. Dean

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

Article abstract of DOI:10.1016/0040-4039(95)02009-E

1,4,7-Triazacyclononane reacts selectively with 2-(t-butoxycarbonyloxyimino)- and 2-(benzyloxycarbonyloxyimino)-2-phenylacetonitrile to give 1,4-diprotected derivatives which could be converted to mono and disubstituted triazacyclononanes.

Full text of DOI:10.1016/0040-4039(95)02009-E

Products guided by the article

Product name:1-Cbz-1,4,7-triazacyclononane

Cas No:174138-02-4

R&D Labs maybe for 174138-02-4

Shanghai Hohance Chemical Co., ltd

Contact:13914753421

Address:Fl.5；Bld. 70, Lane 1500; Xinfei Road
Taizhou KEDE Chemical.Co.,Ltd.

Contact:86-576-84613060

Address:Jiangkou Chemical Zoon
Henan Harvest Chem Co., Ltd

Contact:+86-371-86058576

Address:NO.32, Jingsan Road, Zhengzhou, China
GIHI CHEMICALS CO.,LIMITED

Contact:+86-571-86217390

Address:No.567 Dengcai Street,Sandun,Westlake District,Hangzhou310030,Zhejiang,China.
Wuxi Morality Chemical Co., Ltd(expird)

Contact:

Address:B/7F, 321th WuYun Rd, Wanda Plaza, Wuxi City, 214174, China

Relevant to this article

A facile, one-step conversion of 6-O-trityl and 6-O-TBDMS monosaccharides into the corresponding formate esters

Doi:10.1080/07328300600859668
(2006)
Doi:10.1021/je60035a044
(1967)
Catalytic Decarboxylative Radical Sulfonylation

Doi:10.1016/j.chempr.2020.02.003
(2020)
A useful method for the conversion of olefins to nitro olefins

Doi:10.1021/acs.orglett.1c00868
(2021)
A facile, multigram synthesis of ribofuranoid glycals

Doi:10.1021/jo951376b
(1996)
Aprotic chloride and bromide-promoted alkyne-iminium ion cyclizations

Doi:10.3987/com-95-s96
(1996)

Article Doi