A new efficient and stereoselective synthesis of ubiquinone-10

DOI: 10.1246/bcsj.55.1325

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1325 - 1326 (1982)

Update date:2022-08-05

Topics:

Authors:

Fujita Fujita

Ishiguro

Onishi Onishi

Nishida Nishida

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

Article abstract of DOI:10.1246/bcsj.55.1325

Full text of DOI:10.1246/bcsj.55.1325

Products guided by the article

Product name:6-(4-phenylsulfonyl-3,7,11,15,19,23,27,31,35,39-decamethyl-tetraconta-2,6,10,14,18,22,26,30,34-decaenyl)-2,3-dimethoxy-5-methylhydroquinone bis(2-methoxyethoxymethyl) ether

Cas No:73875-24-8

R&D Labs maybe for 73875-24-8

xujianqiang

Contact:86-21-57725962

Address:shanghai
Suzhou Chiral Pharmaceuticals Co., Ltd.

Contact:86-0512-63197058

Address:Building A, No. 2358, Chang'an Road, Wujiang Science Park
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District
Winchem Industrial Co. Ltd.(expird)

Contact:86-574-83851061 86-574-87083208

Address:Room 905, No.3 Building,East Business Center, 456 Xingning Road, Ningbo City,China
Beijing Cooperate Pharmaceutical Co.,Ltd

website:http://www.cooperate-pharm.com/

Contact:86-01060279497

Address:No.507,Building 4,Tianhua Street, Biomedicine industrial Base

Relevant to this article

Design of 1-substituted 2-arylmethyl-4,5-methylenedioxybenzene derivatives as antiseizure agents

Doi:10.1016/j.bmc.2004.04.015
(2004)
Nucleophilic Addition of N,N'-Dimethylbenzamidine to Activated Double Bonds

Doi:10.1002/ardp.19803130304
(1980)
ROENTGEN CONTRAST MEDIA. 6. IODINATED DERIVATIVES OF

Doi:10.1002/hlca.19650480126
(1965)
Application of the asymmetric aminohydroxylation reaction for the syntheses of HIV-protease inhibitor, hydroxyethylene dipeptide isostere and γ-amino acid derivative

Doi:10.1016/j.tetlet.2004.05.057
(2004)
Synthesis of 2,4-diamino-thieno[2,3-d]pyrimidines

Doi:10.1002/hlca.19900730405
(1990)
Drawing from a pool of radicals for the design of selective enyne cyclizations

Doi:10.1021/ol4028072
(2013)

Article Doi