Triple asymmetric synthesis for fragment assembly: Validity of approximate multiplicativity of the three diastereofacial selectivities
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (52) , 7357-7360
- https://doi.org/10.1016/s0040-4039(00)70696-4
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Synthesis of bryostatins. 1. Construction of the C(1)-C(16) fragmentThe Journal of Organic Chemistry, 1989
- Aldol condensations of chiral ethylketones: Control by chiral boron reagents.Tetrahedron Letters, 1988
- Studies in macrolide synthesis: aldol condensations of chiral ethylketones via boron enolates.Tetrahedron Letters, 1987
- Antineoplastic agents. 126. Isolation and structure of bryostatins 12 and 13The Journal of Organic Chemistry, 1987
- Organoboron compounds in organic synthesis. 4. Asymmetric aldol reactionsJournal of the American Chemical Society, 1986
- Bioactive marine metabolites. Part 16. Calyculin A. A novel antitumor metabolite from the marine sponge Discodermia calyxJournal of the American Chemical Society, 1986
- Isolation and structure of bryostatin 1Journal of the American Chemical Society, 1982
- Stereoselective aldol condensation. Use of chiral boron enolatesJournal of the American Chemical Society, 1981
- Total synthesis of 6-deoxyerythronolide BJournal of the American Chemical Society, 1981
- Antineoplastic Components of Marine AnimalsNature, 1970