Ring cleavage of camphor derivatives: formation of chiral synthons for natural products synthesis
Base-promoted ring cleavage of 9,10- and 8,10-dibromocamphor provides chiral intermediates for natural product synthesis.
Hutchinson, J. H.,Money, T.,Piper, S. E.
p. 854 - 860
(2007/10/02)
A formal enantiospecific synthesis of California red scale pheromone
Cleavage of α,α-disubstituted β-bromoketone intermediates derived from (+)-camphor forms the basis of an alternative enantiospecific synthesis of (Z)-3-methyl-6-isopropenyl-3,9-decadien-1-yl acetate (1), one of the sex pheromones of the female California red scale, Aonidiella aurantii (Maskell).
Hutchinson, John H.,Money, Thomas
p. 3182 - 3185
(2007/10/02)
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