Angewandte Chemie International Edition in English · 1996 · 38 citations · 11 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryReaction EngineeringSynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsStereochemical Optimization1, 2-Addition1, 3-Dipolar CycloadditionAsymmetric Heterocycle SynthesisCycloaddition ReactionsNitrone CycloadditionRing-forming ReactionsStereospecific Reaction Design
Only the convex face of the chiral, cyclic nitrone 1 is accessible to dipolarophiles 2 in [3 + 2] cycloadditions. Since in addition Z2 dictates the orientation of the dipolarophiles by directing the smallest substituent (H) of 2 into the most demanding space, the cycloadducts 3 are obtained with almost perfect stereocontrol.
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Alberto Brandi, Stefano Cicchi, Andrea Goti et al. · The Journal of Organic Chemistry · 1994 · 56 citations