An asymmetric synthesis of aporphine and related alkaloids via chiral formamidines. (+)-Glaucine, (+)-homoglaucine, and (-)-8,9-didemethoxythalisopavine

DOI: 10.1021/jo00308a029

Source and publish data:

Journal of Organic Chemistry p. 5659 - 5662 (1990)

Update date:2022-08-05

Topics: Asymmetric synthesis

Authors:

Gottlieb

Meyers Meyers

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

Article abstract of DOI:10.1021/jo00308a029

Full text of DOI:10.1021/jo00308a029

Products guided by the article

Product name:Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(phenylmethyl)-, (S)-

Cas No:47145-37-9

R&D Labs maybe for 47145-37-9

Changzhou Qidi Chemical Co., Ltd

website:http://www.czqdhg.com/

Contact:86-519-83382137

Address:128-1-16# HuaYuan Street,Hutang Town,Wujin District,Changzhou City,P.R.China.
Jiangsu Chiatai Qingjiang Pharmaceutical Co.,Ltd

Contact:+86-517-86283327

Address:9 North Hantai Road, Huaian, China
Guangzhou PI & PI Biotech Inc. Ltd.

Contact:+86-20-81716320

Address:13th Floor, Xinbao Technology Industrial Park, No. 2 Ruixiang Road, Huangpu District, Guangzhou,Guangdong,China
HUNAN CHEMAPI BIOLOGICAL TECHNOLOGY CO.,LTD.

Contact:+86-186-02659358

Address:1004, building 3, Wanke Jinsemaitianyuan, 498 Guitang Road, Yuhua District, Changsha City, Hunan Province, China
Shanghai Intime pharm Co.,Ltd

Contact:86-21-58226973

Address:No 351,Guoshoujing Road, Zhangjiang Hi-tech Park, Pudong, Shanghai, China

Relevant to this article

A novel C(2)-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester as a promising chiral building block for piperidine-related alkaloids.

Doi:10.1021/ol0265620
(2002)
Highly regioselective construction of spirocycles via phosphine-catalyzed [3 + 2]-cycloaddition

Doi:10.1021/jo026111t
(2002)
A sorbitol dehydrogenase inhibitor of exceptional in vivo potency with a long duration of action: 1-(R)-{4-[4-(4,6-dimethyl[1,3,5]triazin-2-yl)-2R, 6S-dimethylpiperazin-1-yl]pyrimidin-2-yl}ethanol

Doi:10.1021/jm020288y
(2002)
A Novel synthesis of 2-arylpyrrolo[1,2-a]pyrimid-7-ones and their structure-activity relationships as potent GnRH receptor antagonists

Doi:10.1016/S0960-894X(01)00780-6
(2002)
Doi:10.1021/ja01593a023
(1956)
Photodynamic inactivation of Staphylococcus aureus using low symmetrically substituted phthalocyanines supported on a polystyrene polymer fiber

Doi:10.1016/j.dyepig.2012.10.001
(2013)

Article Doi