A chiral analog of the bicyclic guanidine TBD: synthesis, structure and Brønsted base catalysis.

Beilstein J Org Chem

Institute for Organic Chemistry and Chemical Biology, Goethe University Frankfurt, Max-von-Laue-Straße 7, D-60438 Frankfurt am Main, Germany.

Published: August 2016

Starting from ()-β-phenylalanine, easily accessible by lipase-catalyzed kinetic resolution, a chiral triamine was assembled by a reductive amination and finally cyclized to form the title compound . In the crystals of the guanidinium benzoate salt the six membered rings of adopt conformations close to an envelope with the phenyl substituents in pseudo-axial positions. The unprotonated guanidine catalyzes Diels-Alder reactions of anthrones and maleimides (25-30% ee). It also promotes as a strong Brønsted base the retro-aldol reaction of some cycloadducts with kinetic resolution of the enantiomers. In three cases, the retro-aldol products (48-83% ee) could be recrystallized to high enantiopurity (≥95% ee). The absolute configuration of several compounds is supported by anomalous X-ray diffraction and by chemical correlation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082680PMC
http://dx.doi.org/10.3762/bjoc.12.176DOI Listing

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