Xanthocyclines: 5-oxaanthracyclines (7,8,9,10-tetrahydrobenzo[b]xanthen-12-one)
Author(s) -
James L. Charlton,
Vilayat A. Sayeed,
G. N. LYPKA
Publication year - 1982
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/v82-281
Subject(s) - chemistry , daunorubicin , cardiotoxicity , anthracycline , stereochemistry , antibiotics , combinatorial chemistry , pharmacology , organic chemistry , biochemistry , leukemia , toxicity , medicine , cancer , breast cancer
The anthracycline antibiotics daunorubicin and adriamycin are potent antitumor agents. It has recently been suggested that 5-oxaanthracycline analogs of these compounds might show reduced cardiotoxicity, a property that limits the clinical use of the anthracyclines. In this paper we describe the condensation–cyclization reactions of 2-methylchromone-3-carboxylate with cyclohexanones, a reaction that leads ultimately to the xanthocycline skeleton.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom