Total synthesis of muconin
- 25 November 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 43 (48) , 8661-8664
- https://doi.org/10.1016/s0040-4039(02)02182-2
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Stereoselective Synthesis of the 3-Hydroxytetrahydropyran Part of Mucocin, an Antitumor Agent, Based on Rearrangement-Ring Expansion Reaction of a Tetrahydrofuran DerivativeHETEROCYCLES, 2000
- Total Synthesis of (−)-MucocinAngewandte Chemie International Edition in English, 1999
- Enantioselective construction of the tetrahydropyran and tetrahydrofuran fragments of the antitumor agent mucocin from a common intermediateTetrahedron Letters, 1999
- Enantioselective synthesis of the 4-hydroxy buteneolide terminus of mucocin and related annonaceous acetogeninsTetrahedron Letters, 1998
- Total Synthesis of MucocinJournal of the American Chemical Society, 1998
- Unusual bioactive annonaceous acetogenins from Goniothalamus giganteusTetrahedron, 1998
- Jimenezin, a Novel Annonaceous Acetogenin from the Seeds of Rollinia mucosa Containing Adjacent Tetrahydrofuran−Tetrahydropyran Ring Systems,1Journal of Natural Products, 1998
- Stereoselective synthesis of the 2,6-disubstituted tetrahydropyran-3-ol of the potent antitumor agent mucocin via an acyl radical cyclizationTetrahedron Letters, 1997
- Regioselective and stereoselective reductive cleavage of 1,7-dioxaspiro[5.5]undecane alcoholsTetrahedron Letters, 1996
- Mucocin: A New Annonaceous Acetogenin Bearing a Tetrahydropyran RingJournal of the American Chemical Society, 1995