Polycyclic N-hetero compounds. XLIII

DOI: 10.1002/jhet.5570300140

Source and publish data:

Journal of Heterocyclic Chemistry p. 233 - 240 (1993)

Update date:2022-08-05

Topics:

Authors:

Nagamatsu

Hantani Hantani

Sasaki Sasaki

Ohtomo Ohtomo

Nakayama

Hirota Hirota

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

Article abstract of DOI:10.1002/jhet.5570300140

Full text of DOI:10.1002/jhet.5570300140

Products guided by the article

Product name:6,7-dihydro-5H-pyrimido<5,4-d><1>benzazepin-4(3H)-one

Cas No:105895-96-3

R&D Labs maybe for 105895-96-3

Hangzhou Dingyan Chem Co., Ltd

website:http://www.dingyanchem.com

Contact:86-571-87157530

Address:RM.1118,NO.1 Building, Baiyun Tower,Jianggan Area, Hangzhou city, China,310004
Evershine Chemical CO Ltd

Contact:+86-571-87010026

Address:202, Zhenhua Road,
lianyungang jinkang pharmaceutical technology co., ltd.

Contact:008651885445517

Address:Jinshan industrial park, Ganyu county, Lianyungang, Jiangsu Province, 222115, China
Du-Hope International Group

website:http://www.np-chem.com

Contact:0086-25-52346877

Address:199, Jian Ye Road, Nanjing, China
Taizhou Huading Chemical Co.,Ltd(expird)

Contact:+86-576-88583898

Address:Economic&Technology development zone,Taizhou City,Zhejiang Province,China

Relevant to this article

Generation of cyclic ketene-N,X-acetals (X = O, S) from 2-alkyl-1,3-oxazolines and 2-alkyl-1,3-thiazolines. Reactions with acid chlorides, 1,3-diacid chlorides and N-(chlorocarbonyl) isocyanate

Doi:10.1055/s-2005-918499
(2006)
Doi:10.1002/ardp.19763091004
(1976)
Design, synthesis, and structure-affinity relationship studies in NK₁ receptor ligands based on azole-fused quinolinecarboxamide moieties

Doi:10.1016/j.bmc.2008.05.067
(2008)
6-(Diazomethyl)-1,3-bis(methoxymethyl)uracil, synthesis and transformation into annulated pyrimidinediones

Doi:10.1002/hlca.200890132
(2008)
Discovery of imidazole carboxamides as potent and selective CCK1R agonists

Doi:10.1016/j.bmcl.2008.06.057
(2008)
Synthesis and biophysical studies of N2′-functionalized 2′-amino-α-L-LNA

Doi:10.1080/15257770701538841
(2007)

Article Doi