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Synthesis of the diacid sidechain of deoxyharringtonine

โœ Scribed by Joseph Auerbach; Touran Ipaktchi; Steven M. Weinreb


Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
154 KB
Volume
14
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES


Relative configuration of the diacid sid
โœ Touran Ipaktchi; Steven M. Weinreb ๐Ÿ“‚ Article ๐Ÿ“… 1973 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 156 KB

There has been considerable interest in the Ceuhalotaxus alkaloids recently due both to the unusual structure of the parent alkaloid cephalotsxine (7.) and to the promising antileukemia activity of the harringtonines, which are esters of cephalotaxine with severalacyclic dicarboxylic acids. 1-4

Synthesis of deoxyharringtonine
โœ K.L. Mikolajczak; C.R. Smith Jr.; D. Weisleder; T.Ross Kelly; J.C. McKenna; P.A. ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 228 KB
Cyclodextrin sidechain polyesters โ€” synt
โœ Meik Weickenmeier; Gerhard Wenz ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 264 KB

## Abstract An efficient synthesis of a cyclodextrin polymer by a polymerโ€analogous reaction of lithium ฮฒโ€cyclodextrinate with poly[(__N__โ€vinylโ€2โ€pyrrolidinone)โ€__co__โ€(maleic anhydride)] is described. Because cyclodextrin polymer is highly waterโ€soluble, its binding of guests, like 1โ€adamantanami