Synthesis of C-nor emetine pyman

DOI: 10.1248/cpb.40.1390

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1390 - 1397 (1992)

Update date:2022-09-26

Topics:

Authors:

Harada Harada

Okada Okada

Okamura Okamura

Date Date

Ishida Ishida

Takeda Takeda

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Article abstract of DOI:10.1248/cpb.40.1390

The four stereoisomers of C-nor emetine Pyman (2) were synthesized and isolated as their hydrobromides (2a-d·2HBr). Reduction of 3,11b-trans dehydro C-nor emetine Pyman (13a) gave an inseparable mixture of 2a and 2b. They were converted into the correspon

Full text of DOI:10.1248/cpb.40.1390

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Product name:Propanedioic acid, [3-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-3-oxopropyl]-, diethyl ester

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