Ruthenium-catalysed Oxidation of Allyl Alcohols by Molecular Oxygen

DOI: 10.1039/c39810000907

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 907 - 908 (1981)

Update date:2022-08-03

Topics:

Authors:

Matsumoto, Masakatsu

Ito, Satoru

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

Article abstract of DOI:10.1039/c39810000907

Ruthenium(II) catalyses the homogeneous oxidation of allyl alcohols to carbonyl compounds by molecular oxygen under mild conditions.

Full text of DOI:10.1039/c39810000907

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

View Article Online

Products guided by the article

Product name:2-Butenal, 2-methyl-4-(phenylthio)-, (2E)-

Cas No:69690-06-8

R&D Labs maybe for 69690-06-8

Phytomarker Ltd.(expird)

Contact:+86-22-26358246

Address:601-4-20, Fujiayuan, Tiantai Road, Hebei District, Tianjin, China
Zhengzhou Minzhong Pharmaceutical Co.,ltd

Contact:0086-371-65797115

Address:15/F,Jiangshan Bldg, NO.126 Huanghe Road,Zhengzhou, China
Jiangyin Tenghua Import&Export Co.,Ltd.

Contact:+86-510-86263875

Address:Room 402-B,9 Yanling Road, Jiangyin,Jiangsu, China
NANCHANG QINZHI SCI&TEC.CO.,LTD(expird)

Contact:+86-13687004106

Address:Hero South Road,Hero Zone,Nanchang,Jiangxi,China
Advanced Biotech

Contact:+1-973-357-0577

Address:10 Taft Rd.

Relevant to this article

Reactions of 7-methoxyimino-4-methylchromene-2,8-dione with phosphines. Preparation of N-substituted 7-amino-8-hydroxy-4-methyl-2H-[1]-benzopyran-2-ones

Doi:10.1016/0040-4020(96)00923-4
(1996)
Doi:10.1016/S0040-4039(01)94889-0
(1978)
Highly regioselective hydroformylation of 1,5-hexadiene to linear dialdehyde catalyzed by rhodium complexes with tetraphosphorus ligands

Doi:10.1016/j.tetlet.2009.07.066
(2009)
Doi:10.1016/S0040-4039(01)95213-X
(1978)
Formation of incompletely condensed oligosilsesquioxanes by hydrolysis of completely condensed POSS via reshuffling

Doi:10.1246/cl.2008.804
(2008)
Nucleic acid related compounds. 101. S-adenosyl-L-homocysteine hydrolase does not hydrate (5'-fluoro)vinyl or (6'-halo)homovinyl analogues derived from 3'-deoxyadenosine or 3'-(chloro or fluoro)-3'-deoxyadenosine

Doi:10.1021/jo971741u
(1998)

Article Doi