Efficient One-Pot Synthesis of Jm3100
- 1 August 1998
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 28 (15) , 2903-2906
- https://doi.org/10.1080/00397919808004867
Abstract
A facile synthesis of JM3100 was reported. This strategy could also be successfully applied in the cyclen series.Keywords
This publication has 6 references indexed in Scilit:
- Trivalent protecting groups for the synthesis of symmetrical and unsymmetrical bis-tetraazamacrocyclesTetrahedron Letters, 1996
- Antiviral activity of the bicyclam derivative JM3100 against drug-resistant strains of human immunodeficiency virus type 1Antiviral Research, 1996
- A Versatile Intermediate for the Preparation of C-Functionalized Azamacrocycles and Application to the Synthesis of the Potent Anti-HIV Agent (±)JM2936The Journal of Organic Chemistry, 1996
- Synthesis and Structure-Activity Relationships of Phenylenebis(methylene)-Linked Bis-Tetraazamacrocycles That Inhibit HIV Replication. Effects of Macrocyclic Ring Size and Substituents on the Aromatic LinkerJournal of Medicinal Chemistry, 1995
- Stoichiometric Mono N‐Functionalization of Tetraazamacrocycles via Phosphoryl‐Protected IntermediatesAngewandte Chemie International Edition in English, 1991
- Cyclenphosphine oxide. Anomalous member of a homologous seriesJournal of the American Chemical Society, 1983