Stereoselective reactions. XVIII. Synthesis and cytotoxicity of the demethyl derivatives of steganes

DOI: 10.1248/cpb.38.1898

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1898 - 1901 (1990)

Update date:2022-08-04

Topics:

Authors:

Tomioka Tomioka

Kawasaki

Koga Koga

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

Article abstract of DOI:10.1248/cpb.38.1898

Full text of DOI:10.1248/cpb.38.1898

NII-Electronic Library Service

Products guided by the article

Product name:2(3H)-Furanone, 4-(1,3-benzodioxol-5-ylmethyl)dihydro-3-[(3-hydroxy-4,5-dimethoxyphen yl)methyl]-, (3R,4R)-rel-

Cas No:131523-37-0

R&D Labs maybe for 131523-37-0

Hebei Tianxiang Biological & Pharmaceutical Co., Ltd

Contact:86-0312-6615158

Address:No 42 fazhan street qingyuan county
Shanghai PuYi Chem-Tech Co.,Ltd.

Contact:+86-21-57687505-227

Address:3 Floor, Building 11, No 201 MinYi Road, Songjiang District, Shanghai 201612, China
Tianjin Boron PharmaTech Co.,Ltd.(expird)

Contact:86-022-59845187

Address:B9-401, Tianda Science Park,No.80,4th Avenue,TEDA,Tianjin, China
ChengduChroma-BiotechCo.,Ltd.

Contact:86-28-61993785

Address:No.70-13-21, North Section, Erhuan
Nanjing Chemzam Pharmtech Co., Ltd.

Contact:+86-25-86462165,+86-13915979898

Address:C5-1，6 Maiyue Road，Maigaoqiao，Nanjing，Jiangsu，China

Relevant to this article

Aerobic oxidative alkynylation of H-phosphonates and amides: An efficient route for the synthesis of alkynylphosphonates and ynamides using a recyclable Cu-MnO catalyst

Doi:10.1039/c9cy00275h
(2019)
Chiral toluene-2,α-sultam auxiliaries: Asymmetric Diels-Alder reactions of N-enoyl derivatives

Doi:10.1016/S0040-4039(00)97793-1
(1990)
Doi:10.1002/hlca.19490320361
(1949)
Iron-catalyzed reductive dehydroxylation of benzylic alcohols using polymethylhydrosiloxane (PMHS)

Doi:10.1055/s-0031-1289857
(2011)
HYDROBORATION OF P-PHENYL-C,C-BIS(TRIMETHYLSILYLTHIO)METHYLENEPHOSPHINE

Doi:10.1007/BF00958266
(1990)
Local anaesthetic activity of 4-alkoxybenzamides.

Doi:10.1111/j.2042-7158.1955.tb12059.x
(1955)

Article Doi