๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Enantioselective Total Synthesis of Avarol and Avarone

โœ Scribed by Taotao Ling; Alan X. Xiang; Emmanuel A. Theodorakis


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
95 KB
Volume
38
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Stereoselective Syn
โœ J. AN; D. F. WIEMER ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 35 KB ๐Ÿ‘ 1 views

Stereoselective Synthesis of (+)-Avarol, (+)-Avarone, and Some Nonracemic Analogues. -The key step in the synthesis of the title compounds (VIII) and (IX) and the analogue (VII) is Li/NH3-mediated reduction of the enone (III) and subsequent trapping of the intermediate with the bromide (IV). The de

Enantioselective Total Synthesis of Cyli
โœ Nicolai Cramer; Sabine Laschat; Angelika Baro; Harald Schwalbe; Christian Richte ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 108 KB ๐Ÿ‘ 1 views
Enantioselective Total Synthesis of (โˆ’)-
โœ Mohammad Movassaghi; Grazia Piizzi; Dustin S. Siegel; Giovanni Piersanti ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 145 KB

While sesquiterpene illudins M and S (1 and 2, respectively) are highly cytotoxic compounds isolated from Omphalotus illudens, a semisynthetic derivative, (ร€)-irofulven (4; hydroxymethyl acylfulvene (HMAF)), has recently demonstrated far superior efficacy as an antitumor agent. [1, 2] (ร€)-Irofulven