Enantioselective Syntheses and Configuration Assignments of γ??Chiral Butenolides from Plagiomnium undulatum: Butenolide Synthesis from Tetronic Acids
T Kapferer, R Brückner, A Herzig…
Index: Kapferer, Tobias; Brueckner, Reinhard; Herzig, Axel; Koenig, Wilfried A. Chemistry - A European Journal, 2005 , vol. 11, # 7 p. 2154 - 2162
Full Text: HTML
Citation Number: 26
Abstract
Abstract Both enantiomers of the γ-chiral α, β-dimethylated butyrolactones nat-1 and nat-2 from the moss Plagiomnium undulatum were synthesized stereoselectively through butenolides and tetronic acids, respectively. The configuration of the natural products was determined by GLC comparisons with mono (3-O-acetyl-6-O-tert-butyldimethylsilyl-2-O- methyl) hexakis (6-O-tert-butyldimethylsilyl-2, 3-di-O-methyl)-β-cyclodextrin as a stationary ...
Related Articles:
Enzymic condensation of 3-methyl-2-alkenyl pyrophosphates with isopentenyl pyrophosphate
[Ogura,K. et al. Journal of the American Chemical Society, 1970 , vol. 92, p. 6036 - 6041]
[Homsi, Fadi; Rousseau, Gerard Journal of Organic Chemistry, 1999 , vol. 64, # 1 p. 81 - 85]
[Homsi, Fadi; Rousseau, Gerard Journal of Organic Chemistry, 1999 , vol. 64, # 1 p. 81 - 85]
[Okukado,N.; Negishi,E. Tetrahedron Letters, 1978 , # 27 p. 2357 - 2360]