As part of our program on valorisation of moroccan essential oils, we have synthesized, from cis- and trans-himachalenes extracted from cedrus Atlantica, mono and diepoxides in 2,3 and 7,13 or 7,8 position whose configurations were established.
2α,3α:7β,8β-Diépoxy-trans-himachalane
作者:A. Chiaroni、C. Riche、A. Benharref、H. El Jamili、E. Lassaba
DOI:10.1107/s0108270196005768
日期:1996.10.15
The stereochemistry of the major isomer, C(15)H(2)4O(2), resulting from the epoxidation of gamma-trans-himachalene has been established and hence the configurations of the resulting derivatives have been deduced. The seven-membered ring is chair shaped while the six-membered ring adopts a 1,2-diplanar conformation.
Lassaba, E.; Jamili, H. El; Benharref, A., Bulletin des Societes Chimiques Belges, 1997, vol. 106, # 12, p. 773 - 780
作者:Lassaba, E.、Jamili, H. El、Benharref, A.、Chiaroni, A.、Riche, C.、Pierrot, M.
DOI:——
日期:——
Harref, A. Ben; Bernardini, A.; Viallefont, Ph., Journal of Chemical Research, Miniprint, 1981, # 12, p. 4329 - 4356
作者:Harref, A. Ben、Bernardini, A.、Viallefont, Ph.、Fkih-Tetouani, S.、Jacquier, R.