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Boyer and Lallemand

Ferrier carbocyclization can form only cyclohexanones. Nevertheless, chemical manipulations of the latter can provide us with seven-membered rings. This is illustrated by the synthesis of (—)-calystegine B2 by Boyer and Lallemand [305]. These natural polyhydroxylated nortropane compounds are growth stimulators of nitrogen fixing bacteria. [Pg.561]

Soulie, J., Boyer, T. and Lallemand, J.-Y. (1995a). Access to unsaturated chiral epoxides. Part II. Synthesis of a component of the sex pheromone of Phragmatobia fuliginosa. Tetrahedron Asymmetry, 6,625-636. [Pg.443]

See other pages where Boyer and Lallemand is mentioned: [Pg.499]    [Pg.499]    [Pg.499]    [Pg.499]    [Pg.136]    [Pg.341]    [Pg.295]    [Pg.1054]    [Pg.1054]    [Pg.379]    [Pg.323]    [Pg.94]    [Pg.94]    [Pg.674]    [Pg.342]    [Pg.342]    [Pg.295]    [Pg.166]    [Pg.249]    [Pg.94]   
See also in sourсe #XX -- [ Pg.29 , Pg.499 ]



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