Stereocontrolled Total Synthesis of (+)‐Leucascandrolide A
- 20 January 2003
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 115 (3) , 357-361
- https://doi.org/10.1002/ange.200390080
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Synthesis of the C1‘−C11‘Segment of Leucascandrolide AThe Journal of Organic Chemistry, 2001
- Total Synthesis of Leucascandrolide AJournal of the American Chemical Society, 2000
- Catalytic Asymmetric Hetero-Diels–Alder Reactions of Carbonyl Compounds and IminesPublished by Wiley ,2000
- Application of Complex Aldol Reactions to the Total Synthesis of Phorboxazole BJournal of the American Chemical Society, 2000
- Highly Enantio- and Diastereoselective Hetero-Diels-Alder Reactions Catalyzed by New Chiral Tridentate Chromium(III) CatalystsAngewandte Chemie International Edition in English, 1999
- Hochenantio- und -diastereoselektive Hetero-Diels-Alder-Reaktionen, katalyisert durch neue chirale Chrom(III)-KomplexeAngewandte Chemie, 1999
- General Synthesis of α-Acetoxy Ethers from Esters by DIBALH Reduction and AcetylationThe Journal of Organic Chemistry, 1996
- Leucascandrolide A, a New Type of Macrolide: The first powerfully bioactive metabolite of calcareous sponges (Leucascandra caveolata, a new genus from the coral sea)Helvetica Chimica Acta, 1996
- Practical Syntheses of Enantiomerically Enriched γ-Lactones and γ-Hydroxy Ketones by the Alkylation of Pseudoephedrine Amides with Epoxides and Their DerivativesThe Journal of Organic Chemistry, 1996
- A Concise Synthesis of (E)‐ and (Z)‐NeomanoalidesHelvetica Chimica Acta, 1994