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An Efficient Approach to Mechanically Planar Chiral Rotaxanes

[Image: see text] We describe the first method for production of mechanically planar chiral rotaxanes in excellent enantiopurity without the use of chiral separation techniques and, for the first time, unambiguously assign the absolute stereochemistry of the products. This proof-of-concept study, wh...

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Detalles Bibliográficos
Autores principales: Bordoli, Robert J., Goldup, Stephen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977585/
https://www.ncbi.nlm.nih.gov/pubmed/24559064
http://dx.doi.org/10.1021/ja412715m
Descripción
Sumario:[Image: see text] We describe the first method for production of mechanically planar chiral rotaxanes in excellent enantiopurity without the use of chiral separation techniques and, for the first time, unambiguously assign the absolute stereochemistry of the products. This proof-of-concept study, which employs a chiral pool sugar as the source of asymmetry and a high-yielding active template reaction for mechanical bond formation, finally opens the door to detailed investigation of these challenging targets.