Stereoselective Total Synthesis of Cephalosporolide D
- 1 January 2000
- journal article
- Published by CLOCKSS Archive in HETEROCYCLES
- Vol. 52 (3) , 1105
- https://doi.org/10.3987/com-99-s85
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- A New Stereoselective Route to (-)-Octalactin A Based on Intramolecular SmI2 Promoted Reformatsky ReactionSynlett, 1998
- Enantioselective Synthesis of Octalactin AChemistry Letters, 1997
- Studies Directed Toward the Synthesis of Macrolactins: Asymmetric Synthesis of C3-C9and C17-C24Subunits of Macrolactin ASynthetic Communications, 1996
- Convenient Synthesis of (+)-Decarestrictine LChemistry Letters, 1995
- Total Synthesis of (+)-Octalactins A and B: Unusual Metabolites from a Marine MicrobeJournal of the American Chemical Society, 1994
- Effect of Methyl Substituents on the Double Bond Involved in the Formation of Tetrahydropyrans from Hydroxy Allylic AcetatesBulletin of the Chemical Society of Japan, 1994
- Total Synthesis of (+)-Carbonolide BThe Journal of Organic Chemistry, 1994
- Total Synthesis of Grahamimycin A1Bulletin of the Chemical Society of Japan, 1993
- Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes Promoted by the Combined Use of Chiral Diamine Coordinated Tin(II) Triflate and Tributyltin FluorideChemistry Letters, 1989
- Structures of the cephalosporolides B–F, a group of C10lactones from Cephalosporium aphidicolaJournal of the Chemical Society, Perkin Transactions 1, 1985