A direct route to the pyrrolo[2,1-c][1,4]benzodiazepine ring system using aryl triflates
Authors:
- George A. KrausGKGeorge A. Kraus
- Peng LiuPLPeng Liu
- 16 October 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (42) , 7595-7598
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- A direct preparation of 1,4-benzodiazepines. The synthesis of medazepam and related compounds via a common intermediateTetrahedron Letters, 1994
- Synthesis of DNA-Interactive Pyrrolo[2,1-c][1,4]benzodiazepinesChemical Reviews, 1994
- Covalent binding of antitumor antibiotics in the minor groove of DNA. Mechanism of action of CC-1065 and the pyrrolo(1,4)benzodiazepinesAccounts of Chemical Research, 1986
- Design of Sequence-Specific DNA-Binding MoleculesScience, 1986
- Limitations and factors affecting the lactam reduction approach to the synthesis of anthramycin analogsTetrahedron Letters, 1984
- Structural modification of bioactive compounds. II. Syntheses of aminophosphonoic acids.Chemical and Pharmaceutical Bulletin, 1984
- Asymmetrische Synthesen via metallierte chirale Hydrazone. Enantioselektive Alkylierung von cyclischen Ketonen und Aldehyden1European Journal of Inorganic Chemistry, 1979
- 1-Hydroxybenzotriazole as a racemization-suppressing reagent for the incorporation of im-benzyl-L-histidine into peptidesJournal of the American Chemical Society, 1971