Martin P. Schweizer

Nuclear magnetic resonance determination of syn and anti conformations in pyrimidine nucleosides.

Determination of pyrimidine nucleoside syn, anti conformational preference in solution by proton and carbon-13 nuclear magnetic resonance.

Carbon-13 NMR studies of the glycosidic conformation of cytidine and 6-Methylcytidine

The use of proton and carbon-13 nuclear magnetic resonance for assignment of the glycosylation site in 3- and 5-substituted 1- -D-ribofuranosyl-1,2,4-triazoles.

The synthesis of 4-beta-D-ribofuranosyl-as-triazin-3(4H)-one 1-oxide, a potential uridine antagonist.

Synthesis of 6‐amino‐1,2,3‐triazolo[4,5‐c] pyridin‐4(5H)one (8‐aza‐3‐deazaguanine) and 6‐amino‐1‐(β‐D‐ribofuranosyl)‐1,2,3‐triazolo[4,5‐c] pyridin‐4(5H)one (8‐Aza‐3‐deazaguanosine) via novel ring closure procedures

Nucleoside peptides. I. The synthesis of 5'-deoxy-5'-amino-5'-N-aminoacyl peptide derivatives of guanosine, adenosine, and 2'-deoxyadenosine and their effect on cell-free protein synthesis.

Reinvestigation of 3,5'-anhydro-2',3'-O-isopropylideneinosine

THE SYNTHESIS OF 4‐BETA‐D‐RIBOFURANOSYL‐AS‐TRIAZIN‐3(4H)‐ONE 1‐OXIDE, A POTENTIAL URIDINE ANTAGONIST

Additions and Corrections - The Use of Proton and Carbon-13 Nuclear Magnetic Resonance for Assignment of the Glycosylation Site in 3- and 5-Substituted 1-β-D-Ribofuranosyl-1,2,4-triazoles