Facile Cyclization of the Valeronitrile Group Bound to a Nickel Macrocycle

DOI: 10.1021/ja00277a055

Source and publish data:

Journal of the American Chemical Society p. 5353 - 5354 (1986)

Update date:2022-08-05

Topics:

Authors:

Bakac, Andreja

Espenson, James H.

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

Article abstract of DOI:10.1021/ja00277a055

Full text of DOI:10.1021/ja00277a055

Products guided by the article

Product name:{(1R,4R,8S,11S)-1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane}nickel

Cas No:138798-26-2

R&D Labs maybe for 138798-26-2

TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
Guangzhou Swan Chemical Co., Ltd.

Contact:+86-20-31075659

Address:NO.301, Hong ba fang investment BLDG 1,Guan chong village,Shiqi town,Panyu district,Guangzhou
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park
Taizhou YOJOY Chemical Co., Ltd.

Contact:13857143241

Address:Yangfu Industrial Park, Xianju, Zhejiang, P. R. China
Laizhou City Laiyu Chemical CO.,Ltd

Contact:+86-535-2719337/2719339

Address:Chenggang road zhuyou laizhou City Shangdong China

Relevant to this article

Photoredox Synthesis of Arylhydroxylamines from Carboxylic Acids and Nitrosoarenes

Doi:10.1055/s-0036-1591744
(2018)
Chemoselective Staudinger-phosphite reaction of symmetrical glycosyl-phosphites with azido-peptides and polygycerols

Doi:10.1039/c2ob25207d
(2012)
Thromboxane A₂ receptor antagonists. Synthesis and activities of phenylsulfonamido derivatives

Doi:10.1016/0223-5234(91)90009-C
(1991)
Synthesis of novel pyrido[1,2-b][2,4]benzodiazepine derivatives

Doi:10.3184/174751912X13343956275474
(2012)
An easy α-glycosylation methodology for the synthesis and stereochemistry of mycoplasma α-glycolipid antigens

Doi:10.3762/bjoc.8.70
(2012)
Mild construction of 3-methyl tetramic acids enabling a formal synthesis of palau'imide

Doi:10.1021/ol301556a
(2012)

Article Doi