Scholarly article on C19H22N2O3S 56985-26-3 from Journal of the Chemical Society. Chemical communications p. 459

DOI: 10.1039/C3975000459a

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 459 (1975)

Update date:2022-08-16

Topics:

Authors:

Hamon Hamon

Pullen Pullen

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

Article abstract of DOI:10.1039/C3975000459a

Full text of DOI:10.1039/C3975000459a

View Article Online / Journal Homepage / Table of Contents for this issue

Products guided by the article

Product name:C₁₉H₂₂N₂O₃S

Cas No:56985-26-3

R&D Labs maybe for 56985-26-3

TIANJIN FESTO CHEMICAL CO.,LTD(expird)

Contact:86-22-25814570

Address:No.12th,5th Ave.,TEDA,Tianjin,China
Shanghai TBBMed Co.,Ltd

website:http://www.tbbmed.com

Contact:86--21-50498136

Address:Room 6002, Building 7-1, No.160 Basheng Road,Pudong Area,Shanghai China
Shenzhen HwaGen Pharmaceutical Co., Ltd

website:http://www.rafflespt.com

Contact:+86-752-5538396

Address:Guangdong Huizhou China
ANGCHEN BRIGHTCHEM CO., LTD

website:http://www.angchenchem.com

Contact:+86-510-88302099 82327577

Address:Rm. 404/405, Floor 4th, No. 983 FengXiang Road, Wuxi, China
Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi

Relevant to this article

Novel Copper Complexes of Chiral Diphosphines: Preparation, Structure, and Use To Form Rhodium Complex Catalysts for Chiral Hydrogenations

Doi:10.1021/jo01303a016
(1980)
Isolation and structural determination of phepropeptins A, B, C, and D, new proteasome inhibitors, produced by Streptomyces sp.

Doi:10.7164/antibiotics.54.874
(2001)
Synthetic studies on isoquinoline alkaloids. II. Selective conversion of 3,9,10 substituted tetrahydroprotoberberines into 3,9,10 substituted 14 deoxoprotopines. Total synthesis of 3,9,10 substituted 14 deoxoprotopines. Total synthesis of 3,9,10 substitut

Doi:10.1248/cpb.23.2878
(1975)
Doi:10.1039/CT8783300216
()
A Halide-Free Method for Olefin Epoxidation with 30% Hydrogen Peroxide

Doi:10.1246/bcsj.70.905
(1997)
Doi:10.1021/ja01091a031
(1965)

Article Doi

DOI: 10.1039/C3975000459a

Source and publish data: