A Modular Approach to Marine Macrolide Construction. 3. Enantioselective Synthesis of the C1−C28 Sector of Spongistatin 1 (Altohyrtin A)
- 3 February 2000
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 2 (5) , 679-682
- https://doi.org/10.1021/ol0000049
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- Synthesis of the C1−C28 Portion of Spongistatin 1 (Altohyrtin A)The Journal of Organic Chemistry, 1999
- Spongistatins, Cynachyrolides, or Altohyrtins? Marine Macrolides in Cancer TherapyAngewandte Chemie International Edition in English, 1998
- Studies Towards the Synthesis of the C29-C51 Fragment of Altohyrtin ASynlett, 1998
- A Method for Constructing the C18−C28 Dispiroacetal Moiety of Altohyrtin AThe Journal of Organic Chemistry, 1997
- Enantioselective Synthesis of Altohyrtin C (Spongistatin 2): Fragment Assembly and Revision of the Spongistatin 2 Stereochemical AssignmentAngewandte Chemie International Edition in English, 1997
- Enantioselective Synthesis of Altohyrtin C (Spongistatin 2): Synthesis of the EF‐Bis(pyran) SubunitAngewandte Chemie International Edition in English, 1997
- Enantioselective Synthesis of Altohyrtin C (Spongistatin 2): Synthesis of the AB‐ and CD‐Spiroketal SubunitsAngewandte Chemie International Edition in English, 1997
- A Method for Constructing the C2−C12 Dispiroacetal Moiety of Altohyrtin AThe Journal of Organic Chemistry, 1996
- Marine Natural Products. XXXVIII. Absolute Stereostructures of Altohyrtins A, B, and C and 5-Desacetylaltohyrtin A, Potent Cytotoxic Macrolides, from the Okinawan Marine Sponge Hyrtios altum.CHEMICAL & PHARMACEUTICAL BULLETIN, 1996
- Altohyrtins B and C and 5-desacetylaltohyrtin A, potent cytotoxic macrolide congeners of altohyrtin A, from the okinawan marine sponge Hyrtios altum.CHEMICAL & PHARMACEUTICAL BULLETIN, 1993