A formal synthesis of aplasmomycin. Assembly of the c3-c17 segment based on 1,3- and 1,5-asymmetric reductions
- 1 January 1990
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 46 (10) , 3469-3488
- https://doi.org/10.1016/s0040-4020(01)81517-9
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- A Formal Synthesis of Aplasmomycin. Assembly of the C3–C17 Segment Based on Remote Controlled Asymmetric ReductionsChemistry Letters, 1987
- Effect of magnesium cation on high selective 1,5-asymmetric reduction of C2-symmetric acetalketonesTetrahedron Letters, 1987
- Synthetic studies on (+)-aplasmomycin. 2. Stereoselective synthesis of Corey's key intermediate, a formal total synthesisTetrahedron Letters, 1986
- Synthetic studies on (+)-aplasmomycin. 1. Stereoselective synthesis of the C-12~C-17 segmentTetrahedron Letters, 1986
- Total synthesis of (+)-aplasmomycinJournal of the American Chemical Society, 1986
- Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamideTetrahedron, 1984
- Total synthesis of aplasmomycinJournal of the American Chemical Society, 1982
- Total synthesis of aplasmomycin. Stereocontrolled construction of the C(3)-C(17) fragmentJournal of the American Chemical Society, 1982
- Structure of aplasmomycin.The Journal of Antibiotics, 1977
- Studies on marine microorganisms. V. A new antibiotic, aplasmomycin, produced by a streptomycete isolated from shallow sea mud.The Journal of Antibiotics, 1976