Short enantioselective synthesis of (-)-ovalicin, a potent inhibitor of angiogenesis, using substrate-enhanced catalytic asymmetric dihydroxylation

DOI: 10.1021/ja00105a084

Source and publish data:

Journal of the American Chemical Society p. 12109 - 12110 (1994)

Update date:2022-08-04

Topics:

Authors:

Corey Corey

Guzman-Perez, Angel

Noe, Mark C.

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

Article abstract of DOI:10.1021/ja00105a084

Full text of DOI:10.1021/ja00105a084

Products guided by the article

Product name:1-Cyclohexene-1-methanol, 4,4-dimethoxy-

Cas No:72445-27-3

R&D Labs maybe for 72445-27-3

Kunming Biohome Technology Co. Ltd.

website:http://www.biohometech.com/

Contact:86-871-67428869

Address:kunming
henan victory industry co.ltd

Contact:86-371-63655023

Address:No.85,jinshui road,zhengzhou,China
Kaiping Genuine Biochemical Pharmaceutical Co.,Ltd.

Contact:+86-750-2881198

Address:No.1, Xinke Road, Shatang Town, Kaiping, Guangdong Province, P.R.China
Zouping Mingxing Chemical Co.,Ltd.

website:http://www.zoutong.com.cn

Contact:86-543-2240068 2240067

Address:428 Daixi Third Road Zouping County Shandong Province China
Rizhao Lanxing Chemical Indusrial Co.,Ltd

Contact:86-633-2616708

Address:NO.15 West road Shenglan, Lanshan district, Rizhao City

Relevant to this article

Activation of C-H bond by cis-[Pt(NO₃)₂(PPh ₃)₂], cyclometallation of tetramethylthiourea

Doi:10.1016/j.inoche.2003.09.024
(2004)
Synthesis and Enzymatic and Inotropic Activity of Some New 8-Substituted and 6,8-Disubstituted Derivatives of Adenosine Cyclic 3',5'-Monophosphate

Doi:10.1021/jm00177a007
(1980)
Doi:10.1039/c39790000566
(1979)
Multicomponent reactions of 1,3-cyclohexanediones and formaldehyde in glycerol: Stabilization of paraformaldehyde in glycerol resulted from using dimedone as substrate

Doi:10.1002/adsc.200900770
(2010)
Doi:10.1021/ja01199a505
(1947)
Synthesis, photophysical and solvatochromic properties of diacetoxyboron complexes with curcumin derivatives

Doi:10.1016/j.saa.2019.05.031
(2019)

Article Doi