Issue 8, 1987

Synthesis of 3-methyl-6-(2′-hydroxyethyl)-7-formyl-1,8-diethoxyisoquinoline: a key synthon for fredericamycin A

Abstract

Synthesis of an isoquinoline moiety comprising the DEF rings in fredericamycin A has been accomplished in seven steps starting from 4-methyl-5-ethoxyoxazole.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 574-575

Synthesis of 3-methyl-6-(2′-hydroxyethyl)-7-formyl-1,8-diethoxyisoquinoline: a key synthon for fredericamycin A

A. V. R. Rao and D. R. Reddy, J. Chem. Soc., Chem. Commun., 1987, 574 DOI: 10.1039/C39870000574

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