Highly substituted cis-β-cyclopentane amino acids: An approach to the synthesis of trehazolin analogues
- 1 December 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (49) , 7949-7952
- https://doi.org/10.1016/s0040-4039(00)61520-4
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Synthesis and absolute configuration of trehazolin aminocyclitol moietyTetrahedron Letters, 1993
- Synthesis of Racemic and Optically Active Cispentacin (FR109615) Using Intramolecular Nitrone-Olefin Cycloaddition.CHEMICAL & PHARMACEUTICAL BULLETIN, 1993
- Isolation on trehalamine, the aglycon of trehazolin, from microbial broths and characterization of trehazolin related compounds.The Journal of Antibiotics, 1993
- Total Synthesis of Trehalase Inhibitor, TrehazolinChemistry Letters, 1993
- Synthesis of aminocyclitol moieties of trehalase inhibitors, trehalostatin and trehazolin. Confirmation of the correct structure of the inhibitorJournal of the Chemical Society, Perkin Transactions 1, 1992
- Synthesis of aminocyclitol moieties of trehalase inhibitors, trehalostatin and trehazolin. Correct structure of the inhibitorJournal of the Chemical Society, Chemical Communications, 1992
- A reductive aldol strategy for the synthesis of very highly substituted cyclopentanes from sugar lactonesTetrahedron Letters, 1991
- Cispentacin, a new antifungal antibiotic. II. In vitro and in vivo antifungal activities.The Journal of Antibiotics, 1989
- Routes to prostaglandins from sugarsPublished by Walter de Gruyter GmbH ,1983
- Rules for ring closure: application to intramolecular aldol condensations in polyketonic substratesTetrahedron, 1982