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Abstract

Concise synthetic methods for synthesizing 3-carboranyl thymidine analogues (3CTAs) modified with cyclic and acyclic alcohols have been developed. The synthesis of these potential boron neutron capture therapy (BNCT) agents and their preliminary biological evaluation is described.

Keywords

boron neutron capture therapy (BNCT); 3-carboranyl thymidine analogues (3CTAs)

Published in

Nucleosides, Nucleotides and Nucleic Acids
2006, volume: 25, number: 8, pages: 861-866
Publisher: TAYLOR & FRANCIS INC

SLU Authors

UKÄ Subject classification

Veterinary Science
Animal and Dairy Science

Publication identifier

  • DOI: https://doi.org/10.1080/15257770600793844

Permanent link to this page (URI)

https://res.slu.se/id/publ/11231