๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Studies on the total synthesis of the saponaceolides. 2. Enantioselective synthesis of 2-epi-saponaceolide B

โœ Scribed by Giovanni Vidari; Natalina Pazzi; Gianluigi Lanfranchi; Stefano Serra


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
219 KB
Volume
40
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Studies on the total synthesis of the sa
โœ Giovanni Vidari; Gianluigi Lanfranchi; Natalina Pazzi; Stefano Serra ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 214 KB

An asymmetric synthesis of the tricyclic spiroketal subunit of the saponaceolides is described in which the absolute stereochemistry at C-2' and C-6' is established through a conformationally and stereoelectronically controlled cyclization ofa dihydroxyketone pyran intermediate.

ChemInform Abstract: First Total Synthes
โœ Rene Csuk; Stefan Reissmann; Ralph Kluge; Dieter Stroehl; Claudia Korb ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons โš– 40 KB ๐Ÿ‘ 2 views

## Abstract A straightforward synthesis of the title compound (VIII) is elaborated involving a ring closue metathesis as key reaction.