ISSN:
0009-2940
Schlagwort(e):
Oligolactones, macrocyclic
;
Macrocyclization
;
Stannylene template
;
Template synthesis
;
Chemistry
;
Inorganic Chemistry
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
Dibutylstannylene-mediated macrolactonization of methyl 4,6-O-benzylidene-&7alpha;-D-glucopyranoside (2) with glutaryl and phthaloyl dichloride yields the respective dilactones 6e and 6f and parallel tetralactones 5e and 5f as well as the antiparallel tetralactone 4e in the case of glutarylation. The reaction with malonyl dichloride yields a negligible amount of the parallel tetralactone 5d and that of fumaryl and isophthaloyl dichloride yields polyesters only, a byproduct in all these reactions. The mechanism of stannylene-medidted macrolactonization is discussed incorporating data pertaining to known hexa- and octalactone formation when succinyl dichloride is used. A correlation between stannylene dimer symmetry and tetralactone constitutional isomer selectivity is introduced.
Zusätzliches Material:
4 Tab.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/cber.19921250527
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