Anton Copar

发表

Precursor of a β‐lactamase inhibitor: allyl (4S,8S,9R)‐10‐[(E)‐ethylidene]‐4‐methoxy‐11‐oxo‐1‐azatricyclo[7.2.0.03,8]undec‐2‐ene‐2‐carboxylate

T. Šolmajer, T. Mesar, I. Leban, 2002 .

Design, synthesis and bioactivity evaluation of tribactam β lactamase inhibitors

T. Šolmajer, T. Mesar, Mateja Vilar, 2002 .

4-Substituted trinems as broad spectrum beta-lactamase inhibitors: structure-based design, synthesis, and biological activity.

D. Turk, T. Šolmajer, M. Oblak, 2007, Journal of medicinal chemistry.

A new approach for the synthesis of fused pyrroles. The synthesis of acyl substituted pyrrolo[1,2‐x]azines

B. Stanovnik, M. Tiŝler, Anton Copar, 1993 .

Amino acids in the synthesis of heterocyclic compounds. Transformations of thiazolones into imidazole derivatives

B. Stanovnik, M. Tiŝler, Anton Copar, 1992 .

Study on the Preparation of Heteroaryl Substituted Enamines. A Simple Synthesis of Heteroaryl-Substituted Acetaldoximes from Enamines.

B. Stanovnik, M. Tiŝler, Anton Copar, 1996 .

Amino acids in the synthesis of heterocyclic systems. Synthesis of γ‐(5‐(1,2,4‐Triazinylidene))‐α,β‐dehydro‐α‐amino acid derivatives and 6H‐pyrido[1,2‐d][1,2,4]triazin‐6‐ones

B. Stanovnik, M. Tiŝler, Anton Copar, 1995 .

Design, Synthesis and Bioactivity Evaluation of Tribactam β Lactamase Inhibitors (VIII).

T. Šolmajer, T. Mesar, Mateja Vilar, 2002 .

Attempts to prepare some 3‐substituted azolo[1,2‐x]azines, intermediates in the synthesis of azaaplysinopsin derivatives

B. Stanovnik, J. Svete, A. Krbavčič, 1999 .