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2000
Volume 6, Issue 2
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

By means of microwave irradiation, the rearrangement from 12β-tosylate and 12β-alcohol of hecogenin derivatives into C-nor-D-homo-Δ17a(18)-olefin (2) and the Δ13(17a)-isomer (3) was achieved. With this method, the controlled solvolysis in anhydrous pyridine gave total conversion to desired exocyclic-olefin which is expected to be a building block of isosteroidal alkaloids.

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/content/journals/loc/10.2174/157017809787582799
2009-03-01
2025-09-12
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