Synthesis of 2-(3', 4', 5'-Trimethoxybenzoyl)-piperonylic Acid1, 2

WJ Gensler, CM Samour

Index: Gensler; Samour Journal of the American Chemical Society, 1951 , vol. 73, p. 5555

Full Text: HTML

Citation Number: 10

Abstract

The structural relationship between 1-(trimethoxyphenyl)-6, 7-methylenedioxy-3, 4- dihydroisoquinoline (111) and trimethoxybenzoylpiperony lic acid (I) suggested that the former compound might serve in some way as a source for the latter. It became evident, however, that if the transformation of I11 to I were to be effected by oxidation, a structural feature would have to be introduced at the isoquinoline 3-or 4-position which would permit ...

Related Articles:

Synthesis of a Substituted Phenylnaphthalene Related to Podophyllotoxin

[Reeve; Myers Journal of the American Chemical Society, 1953 , vol. 75, p. 4957]

Biaryls in nature: a multi-facetted class of stereochemically, biosynthetically, and pharmacologically intriguing secondary metabolites

[Jackson, David E.; Dewick, Paul M. Phytochemistry (Elsevier), 1984 , vol. 23, # 5 p. 1029 - 1036]

Biaryls in nature: a multi-facetted class of stereochemically, biosynthetically, and pharmacologically intriguing secondary metabolites

[Jackson, David E.; Dewick, Paul M. Phytochemistry (Elsevier), 1984 , vol. 23, # 5 p. 1029 - 1036]

Biaryls in nature: a multi-facetted class of stereochemically, biosynthetically, and pharmacologically intriguing secondary metabolites

[Jackson, David E.; Dewick, Paul M. Phytochemistry (Elsevier), 1984 , vol. 23, # 5 p. 1029 - 1036]

More Articles...