Synthesis 1988; 1988(3): 240-242
DOI: 10.1055/s-1988-27529
communication
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

A Facile Synthesis of (+)-L-Discadenine and its Deuterio Derivatives

Jong-Keun Son* , Kondareddiar Ramalingam, Ronald W. Woodard
  • *Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109-1065, USA
Further Information

Publication History

Publication Date:
20 August 2002 (online)

The synthesis of discadenine, 3-[(3S)-3-amino-3-carboxypropyl] -6-(3-methyl-2-butenyl)-3H-purine, and several of its deuteriated derivatives, which are useful in the study of the stereochemical mechanism of its biosynthesis, have been synthesized in three steps from the appropriate homoserine lactones via a route designed for maximal synthetic versatility. The yields of discadenine obtained from this new route represent a ten-fold increase over previous procedures.

    >