Issue 24, 2001

Diastereoselective synthesis of 5 R and 5 S TT pyrimidine h5(6-4) pyrimidone photoproducts; structural analogues of the mutagenic UV-induced TT (6-4) photolesion

Abstract

Two pyrimidine (6-4) pyrimidone photoproduct derivatives, highly valuable to probe the substituent influence during polymerase replicative bypass, were prepared; one (1a) by diastereoselective Raney nickel reductive desulfurization of the s5(6-4) adduct of TpT (3) and the other (1b) by alkaline treatment of 1a.

Article information

Article type
Communication
Submitted
28 Aug 2001
Accepted
26 Oct 2001
First published
22 Nov 2001

Chem. Commun., 2001, 2550-2551

Diastereoselective synthesis of 5 R and 5 S TT pyrimidine h5(6-4) pyrimidone photoproducts; structural analogues of the mutagenic UV-induced TT (6-4) photolesion

S. K. A. Matus, L. Quintero, J. Fourrey and P. Clivio, Chem. Commun., 2001, 2550 DOI: 10.1039/B107773M

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements