Synthetic studies on nogalamycin : stereospecific C-5 alkylations of a sugar derivative via claisen rearrangement and a new route to 1,1,4-trialkoxybuta-1,3-dienes
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 42 (16) , 4443-4450
- https://doi.org/10.1016/s0040-4020(01)87284-7
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Chiral synthesis of the def-ring system of nogalamycinTetrahedron Letters, 1985
- Nitrone cycloadditions with vinyl silanes: the total synthesis of deoxysugars.Tetrahedron Letters, 1984
- Total synthesis of 2,6-epoxy-2H-1-benzoxocin sugar analogsThe Journal of Organic Chemistry, 1984
- Molecular structure, absolute stereochemistry, and interactions of nogalamycin, a DNA-binding anthracycline antitumor antibioticJournal of the American Chemical Society, 1983
- Total synthesis of C-glycoside fragment of nogalamycinJournal of the Chemical Society, Chemical Communications, 1983
- An improved method for selective substitution on O-3 of D-mannose. Application to the synthesis of methyl 3-O-methyl-and 2-O-α-DmannopyranosidesCarbohydrate Research, 1978
- Structure of nogalamycinJournal of the American Chemical Society, 1977
- Selective formation of 2 esters of some methyl .alpha.-D-hexopyranosides via dibutylstannylene derivativesThe Journal of Organic Chemistry, 1976
- A convenient synthesis of methyl 4,6-O-benzylidene-α- and β-D-allopyranosidesCarbohydrate Research, 1973
- Isolation, characterization and degradation of nogalamycinTetrahedron Letters, 1968