Synthesis p. 715 - 718 (1996)
Update date:2022-08-05
Topics:
Lin, Chu-Chung
Wu, Hsien-Jen
Tetraacetal pentaoxa-cage compounds 4a and 4b and convex oxa-cage compounds 6, 7 and 8 are synthesized from alkylfurans in three steps. Ozonolysis of the endo adducts 2a and 2b in dichloromethane at -78°C followed by reduction with dimethyl sulfide gave the tetraacetal pentaoxa-cages 4a and 4b in 85-90% yields, respectively. Ozonolysis of 2a and 2b in dichloromethane at -78°C followed by treatment with triethylamine gave the convex oxa-cages 6, 7 and 8 in 85-90% yields, respectively. The synthesis of the tetraacetal pentaoxa-cage 12, possessing aromatic substituents directly on the skeleton of the oxa-cages, has also been accomplished.
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