1963
DOI: 10.1002/ardp.19632960404
|View full text |Cite
|
Sign up to set email alerts
|

Derivate von vicinalem Trimethoxybenzol. 2. Mitt.: Amide und Hydrazide der Trimethylgallussäure

Abstract: Ausgangsstoff : 2,O g L-Ephedrin-hydrochlorid (0,Ol Mol). Herstellung wie unter V angegeben. Farblose Kristalle, Loslichkeit wie bei IV. Ausbeute: 1,5 g = 69%. Schmp.L (BthanollWasser) : 64--65O. Schmp.9 (&hanol/Wasser) : 65-66O. Rf = 9.91.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1963
1963
1978
1978

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 9 publications
(1 citation statement)
references
References 20 publications
0
1
0
Order By: Relevance
“…Consequently, this reaction was applied to the synthesis of a,P-epoxy esters which, when exposed to hydrazinolysis and/or aminolysis, yield potentially active hydrazides and amides. a,P-Epoxy amides and hydrazides have been of interest to the authors and others ( 5 ) as potential therapeutic agents. In appropriately substituted glycidic hydrazides, the presence of the epoxide function may .affect the distribution of compounds possessing monoamine oxidase-inhibiting pharmacophores.…”
Section: Cidic Hydrazides Amidesmentioning
confidence: 99%
“…Consequently, this reaction was applied to the synthesis of a,P-epoxy esters which, when exposed to hydrazinolysis and/or aminolysis, yield potentially active hydrazides and amides. a,P-Epoxy amides and hydrazides have been of interest to the authors and others ( 5 ) as potential therapeutic agents. In appropriately substituted glycidic hydrazides, the presence of the epoxide function may .affect the distribution of compounds possessing monoamine oxidase-inhibiting pharmacophores.…”
Section: Cidic Hydrazides Amidesmentioning
confidence: 99%