Scholarly article on (1β)-4α,7,7-Trimethylbicyclo[2.2.1]heptane-2β,3α-diol 28357-12-2 from Bulletin of the Chemical Society of Japan p. 985,989

DOI: 10.1246/bcsj.32.985

Source and publish data:

Bulletin of the Chemical Society of Japan p. 985,989 (1959)

Update date:2022-08-28

Topics:

Authors:

Takeshita

Kitajima

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

Article abstract of DOI:10.1246/bcsj.32.985

Full text of DOI:10.1246/bcsj.32.985

Products guided by the article

Product name:(1β)-4α,7,7-Trimethylbicyclo[2.2.1]heptane-2β,3α-diol

Cas No:28357-12-2

R&D Labs maybe for 28357-12-2

SHANGHAI BIOSUNDRUG CO.,LTD.

Contact:86-21-34622192，13917187091，21-34622765

Address:No. 500 Caobao Road Shanghai P.R China
SHANDONG ZHANHUA YONGHAO PHARMACEUTICAL TECH.CO.,LTD

Contact:+86-576-88685096

Address:GENGJU VILLAGE NORTH ONE KILOMETER,ZHANHUA DISTRICT,BINZHOU CITY,SHANDONG PROVINCE,CHINA.
Nanjing Legend Pharmaceutical & Chemical Co., Ltd.

Contact:+86-25-83767696

Address:14-7 Zhongshan Lu Guluo District, Nanjing
Hubei Onward Bio-Development Co., Ltd.

Contact:+86-718-8417012

Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
LIANYUNGANG YC FINE CHEMICAL CO., LTD

Contact:+86-518-858 99188

Address:Shangdong Modern Bldg, South Greenpark Road, Lianyungang, Jiangsu Pro. China

Relevant to this article

Doi:10.1093/cdj/36.3.212
()
Doi:10.1139/v61-179
(1961)
Measurements of Line Strengths in the HO2 ν₁ Overtone Band at 1.5 μm Using an InGaAsP Laser

Doi:10.1021/j100170a022
(1991)
Asymmetric Synthesis of Lactones with High Enantioselectivity by Intramolecular Carbon-Hydrogen Insertion Reactions of Alkyl Diazoacetates Catalyzed by Chiral Rhodium(II) Carboxamides

Doi:10.1021/ja00023a077
(1991)
Production of amorphadiene in yeast, and its conversion to dihydroartemisinic acid, precursor to the antimalarial agent artemisinin

Doi:10.1073/pnas.1110740109
(2012)
Synthesis, characterization, and nonlinear optical responses of nickel(ii) complexes with phenanthroline-based ligands

Doi:10.1080/00958972.2013.805322
(2013)

Article Doi

DOI: 10.1246/bcsj.32.985