AZO BRIDGES FROM AZINES .21. CARBONYL AND ENOL FUNCTIONALITIES IN PARALLEL POSITIONS TO AZO GROUPS

Authors
Citation
U. Brand et S. Hunig, AZO BRIDGES FROM AZINES .21. CARBONYL AND ENOL FUNCTIONALITIES IN PARALLEL POSITIONS TO AZO GROUPS, Liebigs Annalen, (9), 1996, pp. 1395-1399
Citations number
15
Categorie Soggetti
Chemistry
Journal title
ISSN journal
09473440
Issue
9
Year of publication
1996
Pages
1395 - 1399
Database
ISI
SICI code
0947-3440(1996):9<1395:ABFA.C>2.0.ZU;2-5
Abstract
The synthesis of compounds of type A3, carrying both, a silylenol and an azo grup in parallel rigid positions, and the syntheses of ketone a nd diketone of type B and C, respectively, are reported. The crucial p recursors, the mono- and dihydroxy acetals 2 and 3, both obtained from 1, are transformed by the already reported route to azo compounds 4 a nd 5. The latter compound is also prepared by dihydroxylation of the o lefinic bridge in 7. Swern oxidation of alcohols 4, 6, and 5 yields ke tones 12, 13, and 14. Enol silyl ether 15 (type A3) is obtained from 1 2 via its enolate 17 together with small amounts of diazetidine 16 whi ch may arise from the equilibrium 17 reversible arrow 18 reversible ar row 19. By contrast, cyano ketone 20 yields the enol silyl ether 21 qu antitatively.