A stereoselective synthesis of (±)-homogynolide-B
A highly stereoselective formal total synthesis of homogynolide-B via the ketoketals 4 and the ketospirolactone 3a starting from Hagemann's ester 2 is described. Graphic
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Published in | Tetrahedron letters Vol. 35; no. 3; pp. 429 - 432 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
OXFORD
Elsevier Ltd
17.01.1994
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | A highly stereoselective formal total synthesis of homogynolide-B
via
the ketoketals
4
and the ketospirolactone
3a
starting from Hagemann's ester
2
is described.
Graphic |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/0040-4039(94)85072-0 |