Enantioselective construction of the tetrahydropyran and tetrahydrofuran fragments of the antitumor agent mucocin from a common intermediate
- 1 February 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (7) , 1253-1256
- https://doi.org/10.1016/s0040-4039(98)02674-4
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Temporary Silicon-Tethered Ring-Closing Metathesis Approach to C2-Symmetrical 1,4-Diols: Asymmetric Synthesis of d-AltritolThe Journal of Organic Chemistry, 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
- Combination of the ADH with a Two-dimensional SynthesisSynlett, 1995
- Mucocin: A New Annonaceous Acetogenin Bearing a Tetrahydropyran RingJournal of the American Chemical Society, 1995
- Selective asymmetric dihydroxylation (AD) of dienesJournal of the American Chemical Society, 1992
- Synthesis of the ABC ring system of brevetoxin BJournal of the American Chemical Society, 1989
- Synthetic studies towards the acyltetronic acid iohophore M 139603Tetrahedron Letters, 1986
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Alkaloid synthesis by the intramolecular imino Diels-Alder reaction. .delta.-Coniceine and tylophorineJournal of the American Chemical Society, 1979