Autor: |
Puppala, Manohar, Gore, Sangram, Eyong, Kenneth O., Baskaran, Sundarababu |
Předmět: |
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Zdroj: |
European Journal of Organic Chemistry; 5/12/2023, Vol. 26 Issue 19, p1-8, 8p |
Abstrakt: |
A concise approach has been developed for the diastereoselective synthesis of the azatricyclic core of (−)‐7 a‐epi‐lepadiformine A (8 a) and (−)‐7 a‐epi‐lepadiformine C (8 b) using stereoselective domino semipinacol‐Schmidt reaction as a key step. In presence of TiCl4, the oxaspiropentane‐azide derivatives underwent stereoselective domino cyclization to furnish the corresponding angularly fused azatricyclic cores in very good yields. Moreover, azatricyclic core of (−)‐7 a‐epi‐lepadiformine A has also been realized, in a stepwise manner, through the intramolecular Schmidt reaction of azido‐spirocyclobutanone intermediate. The synthetic utility of domino semipinacol‐Schmidt reaction is further shown in the diastereoselective synthesis of (+)‐7 a‐epi‐lepadiformine C (7). [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
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