TY - JOUR
T1 - The Final Stereogenic Unit of [2]Rotaxanes
T2 - Type 2 Geometric Isomers
AU - Savoini, Andrea
AU - Gallagher, Peter R.
AU - Saady, Abed
AU - Goldup, Stephen M.
N1 - Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society
PY - 2024/3/27
Y1 - 2024/3/27
N2 - Mechanical stereochemistry arises when the interlocking of stereochemically trivial covalent subcomponents results in a stereochemically complex object. Although this general concept was identified in 1961, the stereochemical description of these molecules is still under development to the extent that new forms of mechanical stereochemistry are still being identified. Here, we present a simple analysis of rotaxane and catenane stereochemistry that allowed us to identify the final missing simple mechanical stereogenic unit, an overlooked form of rotaxane geometric isomerism, and demonstrate its stereoselective synthesis.
AB - Mechanical stereochemistry arises when the interlocking of stereochemically trivial covalent subcomponents results in a stereochemically complex object. Although this general concept was identified in 1961, the stereochemical description of these molecules is still under development to the extent that new forms of mechanical stereochemistry are still being identified. Here, we present a simple analysis of rotaxane and catenane stereochemistry that allowed us to identify the final missing simple mechanical stereogenic unit, an overlooked form of rotaxane geometric isomerism, and demonstrate its stereoselective synthesis.
UR - http://www.scopus.com/inward/record.url?scp=85186574415&partnerID=8YFLogxK
U2 - 10.1021/jacs.3c14594
DO - 10.1021/jacs.3c14594
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C2 - 38499387
AN - SCOPUS:85186574415
SN - 0002-7863
VL - 146
SP - 8472
EP - 8479
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 12
ER -