Synthetic studies on cardiovascular agents. IV. Synthesis of fused dihydropyridine derivatives

DOI: 10.1248/yakushi1947.98.4_448

Source and publish data:

Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan p. 448 - 465 (1978)

Update date:2022-08-04

Topics:

Authors:

Sato Sato

Shimoji Shimoji

Fujita Fujita

Mizuno Mizuno

Kumakura

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

Article abstract of DOI:10.1248/yakushi1947.98.4_448

Full text of DOI:10.1248/yakushi1947.98.4_448

NII-Electronic Library Service

Products guided by the article

Product name:2-methyl-7-oxo-4-phenyl-6-(3,4,5-trimethoxy-benzyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid ethyl ester

Cas No:67043-57-6

R&D Labs maybe for 67043-57-6

Beijing Pure Chem Co.,Ltd.

Contact:+86-10-83993285

Address:Rm.1708, Haobai Tower, Building 6, No.50, North Road, West Third Ring, Haidian District, Beijing, China
Taizhou Huading Chemical Co.,Ltd(expird)

Contact:+86-576-88583898

Address:Economic&Technology development zone,Taizhou City,Zhejiang Province,China
MedicalChem(Yancheng)Manuf.Co.,Ltd.

Contact:+86-515-84383366

Address:Touzeng BinHai, YanCheng City, JiangSu Province, China
GIHI CHEMICALS CO.,LIMITED

Contact:+86-571-86217390

Address:No.567 Dengcai Street,Sandun,Westlake District,Hangzhou310030,Zhejiang,China.
Jinan Decheng Hemu Medical Technology Co.，Ltd.

Contact:+86-531-68650525

Address:NO.554 Zhengfeng Road High-new Technology Development Zone

Relevant to this article

Synthesis and structure-activity relationships of retinoid X receptor selective diaryl sulfide analogs of retinoic acid

Doi:10.1021/jm960386h
(1996)
Synthesis of N²-alkyl(aryl, dialkyl, cycloalkyl)guanines

Doi:10.1007/bf01169255
(1996)
Doi:10.1021/ja01120a047
(1953)
Doi:10.1021/jo00820a011
(1971)
Doi:10.1016/0022-328X(68)80084-1
(1968)
Development of a Quality Controllable and Scalable Process for the Preparation of 7,8-Difluoro-6,11-dihydrodibenzo[ b, e]thiepin-11-ol: A Key Intermediate for Baloxavir Marboxil

Doi:10.1021/acs.oprd.9b00389
(2019)

Article Doi