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The synthesis of intramolecularly hydrogen-bonded dendrons with stereogenic terminal groups derived from (1S,2S)-(+)-thiomicamine up to the third generation is described. Circular dichroism (CD) studies reveal that the equilibria interconverting two diastereomeric helical conformations (M and P helices) relating a pair of anthranilamide termini depends on solvent, temperature, and dendrimer generation. A conformational preference for M-type helicity along the periphery of the dendrons increased with increasing dendrimer generation and in poor solvents as observed by CD. Equilibration of these diastereomeric helical conformations is rapid at the first generation in all solvents and at all temperatures investigated; however, at the second generation the equilibrium begins to bias a single diastereomeric helical conformation along the periphery that becomes maximal at low temperatures and in poor solvents. At the third generation, the helical bias is intrinsically higher so that the conformational preference...

An efficient route to various sugar lactones has been developed. Key to the overall transformation is the sequential osmium-catalyzed dihydroxylation of 2,4-dienoates. The simplest (one-step/racemic) example of this reaction occurs when the dihydroxylation is performed with aqueous NMO in MeOH. When the first dihydroxylation is performed using the AD-mix procedure, an enantioselective variant results. When a matched AD-mix procedure is used for the second dihydroxylation, an exceedingly diastereo- and enantioselective synthesis of galacto-1,4-lactone results. [Reaction: see text]

An efficient route to various sugar lactones has been developed. Key to the overall transformation is the sequential osmium-catalyzed dihydroxylation of 2,4-dienoates. The simplest (one-step/racemic) example of this reaction occurs when the dihydroxylation is performed with aqueous NMO in MeOH. When the first dihydroxylation is performed using the AD-mix procedure, an enantioselective variant results. When a matched AD-mix procedure is used for the second dihydroxylation, an exceedingly diastereo- and enantioselective synthesis of galacto-1,4-lactone results. [Reaction: see text]