LEADER 01135nam0 2200289 i 450 001 SUN0018700 005 20140625025023.238 010 $a15-667-0092-2 100 $a20040702d1996 |0engc50 ba 101 $aeng 102 $aGB 105 $a|||| ||||| 200 1 $aCoastal zone management handbook$fJohn R. Clark 210 $aBoca Raton$aLondon$cCRC$d1996 215 $a694 p.$cill.$d27 cm. 620 $aGB$dLondon$3SUNL000015 676 $a333.784$v21 700 1$aClark$b, John R.$3SUNV014787$0444139 712 $aCRC$3SUNV000167$4650 790 1$aClark, J. R.$zClark, John R.$3SUNV014789 790 1$aClark, John Russel$zClark, John R.$3SUNV051984 801 $aIT$bSOL$c20201221$gRICA 912 $aSUN0018700 950 $aUFFICIO DI BIBLIOTECA DEL DIPARTIMENTO DI INGEGNERIA$d05CONS G V 151 $e05 3784 20040702 950 $aUFFICIO DI BIBLIOTECA DEL DIPARTIMENTO DI INGEGNERIA$d05CONS G V 349 $e05UBI170 20151201 996 $aCoastal zone management handbook$996798 997 $aUNICAMPANIA LEADER 02165nam 2200361 n 450 001 996396293803316 005 20221108040802.0 035 $a(CKB)4330000000330886 035 $a(EEBO)2240918644 035 $a(UnM)99839892 035 $a(EXLCZ)994330000000330886 100 $a19910116d1590 uy | 101 0 $aeng 135 $aurbn||||a|bb| 200 12$aA treatise against vvitchcraft: or A dialogue, wherein the greatest doubts concerning that sinne, are briefly answered$b[electronic resource] $ea Sathanicall operation in the witchcraft of all times is truly prooued: the moste precious preseruatiues against such euils are shewed: very needful to be knowen of all men, but chiefly of the masters and fathers of families, that they may learn the best meanes to purge their houses of all vnclean spirits, and wisely to auoide the dreadfull impieties and greate daungers which come by such abhominations. Hereunto is also added a short discourse, containing the most certen meanes ordained of God, to discouer, expell, and to confound all the Sathanicall inuentions of witchcraft and sorcerie 210 $aCambridge $cPrinted by Iohn Legatt, printer to the Vniuersitie of Cambridge$d1590 215 $a[64], 24 p 300 $aDedication signed: Henr. Holland. 300 $aSignatures: A-L?. 300 $a"A short discourse shewing the most certen and principal meanes ordeined of God to discouer, expell, and to confound all the Sathanicall inuentions of witchcraft and sorcerie" has separate divisional title page on H4v and separate pagination starting on I1r; register is continuous. 300 $aReproduction of the original in the Henry E. Huntington Library and Art Gallery. 330 $aeebo-0113 606 $aWitchcraft$vEarly works to 1800 615 0$aWitchcraft 700 $aHolland$b Henry$f1555 or 6-1603.$01005456 801 0$bCu-RivES 801 1$bCu-RivES 801 2$bCStRLIN 801 2$bWaOLN 906 $aBOOK 912 $a996396293803316 996 $aA treatise against vvitchcraft: or A dialogue, wherein the greatest doubts concerning that sinne, are briefly answered$92311701 997 $aUNISA 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