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dc.contributor.authorLi, WSen_US
dc.contributor.authorChung, WSen_US
dc.contributor.authorChao, Ien_US
dc.date.accessioned2014-12-08T15:41:18Z-
dc.date.available2014-12-08T15:41:18Z-
dc.date.issued2003-02-17en_US
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://dx.doi.org/10.1002/chem.200390117en_US
dc.identifier.urihttp://hdl.handle.net/11536/28090-
dc.description.abstractThe use of a cyclodextrin . Diels-Alder transition structure complex (CD . TS) as a model in molecular dynamics simulations has enabled us to gain insight into the controlling factors in the cyclodextrin-mediated Diels-Alder reaction of methyl-p-benzoquinone with isoprene. MD Simulations were carried out with multiple binding configurations of the CD . TS (TS = meta-TS, para-TS) complexes at the top and bottom rims of beta-CD. We discovered that i) only shallow binding with the CD is necessary for the regioselectivity, and multiple binding geometries are possible: ii) the narrow bottom rim. with the primary hydroxyl groups, of the CD binds both regio-TSs better than at the wider top rim (secondary hydroxyl groups), which was unexpected from the perspective of shape complementarity that governs the stability of most CD . guest complexes. Overall, the bottom rim of the CD exhibits higher regioisomer discrimination for the meta-TS; iii) structural clustering analyses of the CD . TS configurations (sampled during MD simulations) have enabled us to evaluate the binding energies of the different binding configurations. The result indicates that there is a direct correlation between meta-product selectivity and a higher number of binding configurations favoring the formation of the CD . meta-TS complex, The main forces of stabilization in the CD . TS complexes are the van der Waals interactions when the TS is bound at the top rim. At the bottom rim, closer contacts between polar functional groups of the TS and CD have increased the importance of electrostatic interactions, We found that van der Waals, solvation, and torsional forces are less favorable for complexation at the bottom rime however, this is compensated by large favorable electrostatic interactions. With insights obtained from the study of CD . TS complexes and MD simulations of the modified heptakis-[6-O-(2-hydroxyl)propyl]-beta-CD, we were able to explain why a low selectivity was observed when the Diels-Alder reaction was carried out in this modified CD. Two types of search method [Monte Carlo and multiple minimum (MCMM) and molecular dynamics (MD)] to explore and evaluate the different possible binding geometries of the TS within beta-CD, were discussed.en_US
dc.language.isoen_USen_US
dc.subjectcycloadditionsen_US
dc.subjectcyclodextrinen_US
dc.subjectmolecular dynamics calculationsen_US
dc.subjecttransition structureen_US
dc.titleA computational study of regioselectivity in a cyclodextrin-mediated Diels-Alder reaction: Revelation of site selectivity and the importance of shallow binding and multiple binding modesen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/chem.200390117en_US
dc.identifier.journalCHEMISTRY-A EUROPEAN JOURNALen_US
dc.citation.volume9en_US
dc.citation.issue4en_US
dc.citation.spage951en_US
dc.citation.epage962en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000181131300015-
dc.citation.woscount6-
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