LEADER 03566nam 22006735 450 001 9910743395103321 005 20251204110604.0 010 $a981-16-7430-2 010 $a981-16-7431-0 010 $a981-16-7431-0 024 7 $a10.1007/978-981-16-7431-0 035 $a(MiAaPQ)EBC6810941 035 $a(Au-PeEL)EBL6810941 035 $a(CKB)19919344300041 035 $a(OCoLC)1287130633 035 $a(PPN)258840471 035 $a(BIP)81700825 035 $a(DE-He213)978-981-16-7431-0 035 $a(EXLCZ)9919919344300041 100 $a20211118d2022 u| 0 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aDiscrimination of Mobile Supramolecular Chirality $eAcylative Molecular Transformations by Organocatalysis /$fby Ayumi Imayoshi 205 $a1st ed. 2022. 210 1$aSingapore :$cSpringer Nature Singapore :$cImprint: Springer,$d2022. 215 $a1 online resource (99 pages) 225 1 $aSpringer Theses, Recognizing Outstanding Ph.D. Research,$x2190-5061 311 08$aPrint version: Imayoshi, Ayumi Discrimination of Mobile Supramolecular Chirality Singapore : Springer Singapore Pte. Limited,c2021 9789811674303 327 $aIntroduction -- Mechanistic Study of Organocatalytic Chemoselective Monoacylation of 1,5-Pentanediol -- Discrimination of Mobile Supramolecular Chirality: Kinetic Resolution of Topologically Chiral Racemic Rotaxanes by Organocatalysis -- Conclusion and Perspective. 330 $aThis book proposes a novel concept for molecular recognition. In the field of asymmetric synthesis approaching the mature science, asymmetric discrimination and catalytic synthesis of chiral supramolecules still stand as unsolved problems. The extreme difficulty in asymmetric synthesis of such supramolecules may result from the mobile nature of supramolecular chirality. Here the author shows the first highly enantioselective synthesis of mechanically chiral supramolecules. In the presence of a chiral organocatalyst, a mechanically planar chiral rotaxane was obtained with p erfect enantiopurity (>99% ee) with an excellent selectivity. The dynamic and flexible recognition mode enabled asymmetric synthesis of supramolecules with conformational flexibility and mobility. The recognition mode of the catalyst is a contrast to the traditional static and rigid recognition mode of the typical conventional catalysts. The concept of dynamic molecular recognition will be adopted as a novel concept in a wide range of fields beyond the field of organic chemistry, including material chemistry, biochemistry, and medicinal chemistry. 410 0$aSpringer Theses, Recognizing Outstanding Ph.D. Research,$x2190-5061 606 $aChemistry, Organic 606 $aCatalysis 606 $aNanotechnology 606 $aClinical biochemistry 606 $aOrganic Chemistry 606 $aCatalysis 606 $aNanotechnology 606 $aMedical Biochemistry 615 0$aChemistry, Organic. 615 0$aCatalysis. 615 0$aNanotechnology. 615 0$aClinical biochemistry. 615 14$aOrganic Chemistry. 615 24$aCatalysis. 615 24$aNanotechnology. 615 24$aMedical Biochemistry. 676 $a541.226 700 $aImayoshi$b Ayumi$01077385 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910743395103321 996 $aDiscrimination of Mobile Supramolecular Chirality$92588761 997 $aUNINA