Synthesis of (3S, 4S)-4-hydroxy-2, 3, 4, 5-tetrahydropyridazine-3-carboxylic acid, component of luzopeptin A.
- 1 August 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (8) , 1989-1994
- https://doi.org/10.1016/0957-4166(95)00258-q
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Stereoselective Organic Synthesis via Dynamic Kinetic ResolutionBulletin of the Chemical Society of Japan, 1995
- Enantioselective hydrogenation reactions with a full set of preformed and prepared in situ chiral diphosphine-ruthenium (II) catalysts.Tetrahedron: Asymmetry, 1994
- Asymmetric Synthesis of AntiN-Boc-α-Hydrazino-β-Hydroxyesters from β-Ketoesters by Sequential Catalytic Hydrogenation and Electrophilic AminationSynlett, 1993
- Enantioselective reduction of β-keto estersTetrahedron Letters, 1991
- Useful Syntheses of (3S)-2,3,4,5-Tetrahydropyridazine-3-carboxylic Acid and Its Dehydrotetrapeptide DerivativesChemistry Letters, 1991
- Total synthesis of 3(S)-carboxy-4(S)-hydroxy-2,3,4,5-tetrahydropyridazine, an unusual amino acid constituent of luzopeptin AThe Journal of Organic Chemistry, 1989
- Studies of cirratiomycins. Part II. The structures of cirratiomycin A and B, the new peptide antibiotics.Agricultural and Biological Chemistry, 1982
- Crystal and molecular structure of BBM-928 A, a novel antitumor antibiotic from Actinomadura luzonensisJournal of the American Chemical Society, 1981
- BBM-928, a new antitumor antibiotic complex I. Production, isolation, characterization and antitumor activity.The Journal of Antibiotics, 1980
- C‐Acylation under Virtually Neutral ConditionsAngewandte Chemie International Edition in English, 1979