The use of the Strecker reaction for the synthesis of sympathomimetic amine analogues and their cis-Pt(II) complexes

DOI: 10.1016/0223-5234(87)90270-4

Source and publish data:

European Journal of Medicinal Chemistry p. 325 - 329 (1987)

Update date:2022-08-06

Topics:

Authors:

Haroutounian

Georgiadis

Delitheos

Bailar Jr.

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

Article abstract of DOI:10.1016/0223-5234(87)90270-4

Full text of DOI:10.1016/0223-5234(87)90270-4

Products guided by the article

Product name:1-N-benzylamino-(2-phenyl-cyclohexyl) carbonitrile

Cas No:125659-96-3

R&D Labs maybe for 125659-96-3

Xi'an Galaxy Chemicals CO., Ltd

Contact:86-29-89380370

Address:No.8, Gaoxin three road, Xi'an city.
Jinhua Haoyuan Chemical CO., LTD(expird)

Contact:86-579-82465583

Address:Jinhua,Zhejiang
KINHENG CHEMICAL(SHANGHAI)CO., LTD.

Contact:+8621-60490170

Address:Room401, No.28,Lane 189, Yangshupu Rd. Shanghai, China.
HuiFeiChem PharmaTech Co.Ltd

Contact:0510-85393305

Address:1619 Huishan Avenue, Huishan District, Wuxi,
FUJIAN SHANSHUI CHEMICAL CORP.LTD.

Contact:+86-151-59920036

Address:Jinqiao Gareden, jo@fj-xinyi.com

Relevant to this article

Stereochemical Course of the Transannular Cyclization, in Chloroform, of Epoxycembranoids Derived from the Geometrical Isomers of (14S)-14-Hydroxy-1,3,7,11-cembratetraenes

Doi:10.1021/jo00293a049
(1990)
Synthesis of {15-benzyloxy-3,7,11,17-tetraazabicyclo[11.3.1]heptadeca-1(17) ,13,15-triene}nickel(II) perchlorate and its analogs, and their catalytic behavior in reductive debromination of 1-bromo-4-tert-butylbenzene

Doi:10.1016/j.ica.2010.05.051
(2010)
Bidentate P, N-P ligand for nickel-catalyzed cross-coupling of aryl or benzyl chlorides with ArMgX

Doi:10.1021/jo1016458
(2010)
Synthesis of new pyrazole derivatives and their anticancer evaluation

Doi:10.1016/j.ejmech.2010.07.064
(2010)
Silica-immobilized chiral dirhodium(II) catalyst for enantioselective carbenoid reactions

Doi:10.1021/ol403006r
(2013)
Polyyne Rotaxanes: Stabilization by Encapsulation

Doi:10.1021/jacs.5b12049
(2016)

Article Doi