A novel type of unsaturated seconucleoside analogues

3Citations
Citations of this article
2Readers
Mendeley users who have this article in their library.
Get full text

Abstract

1′,2′-Unsaturated secoadenosine 3-6 and secouridine 15, 16 analogues were synthesized by the base promoted regioselective elimination of corresponding 2′,3′-ditosylates. Efficient and selective O-detritylation of these acid sensitive compounds was achieved by ZnBr2 in dichloromethane. © 1994.

Cite

CITATION STYLE

APA

Vrček, V., & Čaplar, V. (1994). A novel type of unsaturated seconucleoside analogues. Tetrahedron Letters, 35(23), 3987–3990. https://doi.org/10.1016/S0040-4039(00)76721-9

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free