Total syntheses of the sesquiterpenoids (+)-trans-dracunculifoliol and (+)-4-hydroxyoppositan-7-one
RM Oballa, R Carson, S Lait, JA Cadieux, J Robichaud
Index: Oballa, Renata M.; Carson, Rebekah; Lait, Susan; Cadieux, Jay A.; Robichaud, Joel Tetrahedron, 2005 , vol. 61, # 11 p. 2761 - 2766
Full Text: HTML
Citation Number: 4
Abstract
Sesquiterpenoids (+)-trans-dracuncuflifoliol () and (+)-4-hydroxyoppositan-7-one () were prepared stereoselectively from enantiomerically pure (7aR)-7a-methyl-1, 2, 5, 6, 7, 7a- hexahydro-4H-inden-4-one (), whose synthesis was described herein. Conjugate addition of the organocopper (I) reagent to, followed by epimerization of the ring junction, generated 3 of the 4 contiguous chiral centers of both natural products.
Related Articles:
[Salomon; Sachinvala; Roy; Basu; Raychaudhuri; Miller; Sharma Journal of the American Chemical Society, 1991 , vol. 113, # 8 p. 3085 - 3095]
[Johnson, Carl R.; Barbachyn, Michael R. Journal of the American Chemical Society, 1982 , vol. 104, # 15 p. 4290 - 4291]
[Frings, Marcus; Thome, Isabelle; Bolm, Carsten Beilstein Journal of Organic Chemistry, 2012 , vol. 8, p. 1443 - 1451]
[Johnson,C.R.; Corkins,H.G. Journal of Organic Chemistry, 1978 , vol. 43, p. 4136 - 4140]
[Johnson, Carl R.; Barbachyn, Michael R. Journal of the American Chemical Society, 1982 , vol. 104, # 15 p. 4290 - 4291]