LEADER 00916nam0-22003011i-450 001 990004464690403321 005 20210928101947.0 035 $a000446469 035 $aFED01000446469 035 $a(Aleph)000446469FED01 035 $a000446469 100 $a19990530d1920----km-y0itay50------ba 101 0 $aita 105 $ay-------001yy 200 1 $aNote di guerra$fLuigi Capello 210 $aMilano$cFratelli Treves$d1920 215 $a2 v.$d20 cm 327 $1001000112912$12001$a1.: Dall'inizio alla presa di Gorizia 327 $1001000112913$12001$a2.: Vodice - Bainsizza . Caporetto - la vittoria finale 700 1$aCapello,$bLuigi$0136909 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990004464690403321 952 $a4/ III F 10$bbibl.6869/3147$fFLFBC 952 $a4/ III F 11$bbibl.7174/3465$fFLFBC 959 $aFLFBC 996 $aNote di guerra$9545188 997 $aUNINA LEADER 01196nam 2200349Ia 450 001 996396728303316 005 20221108084804.0 035 $a(CKB)4330000000330367 035 $a(EEBO)2240956440 035 $a(OCoLC)12219735 035 $a(EXLCZ)994330000000330367 100 $a19850701d1697 uy | 101 0 $aeng 135 $aurbn#|||a|bb| 200 12$aA letter in answer to a book entitled, Christianity not mysterious$b[electronic resource] $eas also, to all those who set up for reason and evidence in opposition to revelation & mysteries /$fby Peter Browne .. 210 $aDublin $cPrinted by Joseph Ray ... for John North ...$d1697 215 $a[4], 231, [1] p 300 $aErrata: p. [1] at end. 300 $aReproduction of original in British Library. 330 $aeebo-0018 606 $aDeism$vControversial literature 615 0$aDeism 700 $aBrowne$b Peter$fapproximately 1666-1735.$01214978 801 0$bEAA 801 1$bEAA 801 2$bm/c 801 2$bUMI 801 2$bWaOLN 906 $aBOOK 912 $a996396728303316 996 $aA letter in answer to a book entitled, Christianity not mysterious$92806225 997 $aUNISA LEADER 01314nas 2200373-a 450 001 9910891412303321 005 20240413015111.0 035 $a(CKB)2560000000094790 035 $a(CONSER)--2012273295 035 $a(DE-599)ZDB2760788-4 035 $a(EXLCZ)992560000000094790 100 $a20060920a20049999 --- - 101 0 $aeng 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aDidactics of mathematics 210 $aWroclaw $cPublishing House of the Wroclaw University of Economics$d2004- 215 $a1 online resource 300 $aRefereed/Peer-reviewed 311 08$aPrint version: Didactics of mathematics. 1733-7941 (DLC) 2012273295 (OCoLC)71367399 606 $aMathematics$xStudy and teaching$vPeriodicals 606 $aMathématiques$xÉtude et enseignement$vPériodiques 606 $aMathematics$xStudy and teaching$2fast$3(OCoLC)fst01012236 608 $aPeriodicals.$2fast 615 0$aMathematics$xStudy and teaching 615 6$aMathématiques$xÉtude et enseignement 615 7$aMathematics$xStudy and teaching. 712 02$aUniwersytet Ekonomiczny we Wroc?awiu. 906 $aJOURNAL 912 $a9910891412303321 920 $aexl_impl conversion 996 $aDidactics of mathematics$94271423 997 $aUNINA LEADER 05263nam 2200673Ia 450 001 9911020332203321 005 20200520144314.0 010 $a9786612461071 010 $a9781282461079 010 $a1282461079 010 $a9780470747957 010 $a0470747951 010 $a9780470747933 010 $a0470747935 035 $a(CKB)1000000000822301 035 $a(EBL)470758 035 $a(OCoLC)476311784 035 $a(SSID)ssj0000336424 035 $a(PQKBManifestationID)11229534 035 $a(PQKBTitleCode)TC0000336424 035 $a(PQKBWorkID)10281868 035 $a(PQKB)10465452 035 $a(MiAaPQ)EBC470758 035 $a(Perlego)2756899 035 $a(EXLCZ)991000000000822301 100 $a20090827d2009 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCumulenes in click reactions /$fHenri Ulrich 210 $aHoboken, NJ $cWiley$d2009 215 $a1 online resource (566 p.) 300 $aDescription based upon print version of record. 311 08$a9780470779323 311 08$a0470779322 320 $aIncludes bibliographical references and index. 327 $aCumulenes in Click Reactions; Contents; Preface; Acknowledgements; 1 General Introduction; References; 2 1-Carbon Cumulenes; 2.1 Sulfines, R2C SO; 2.1.1 Introduction; 2.1.2 Dimerization Reactions; 2.1.3 Cycloaddition Reactions; References; 2.2 Sulfenes, R2C S(O)O; 2.2.1 Introduction; 2.2.2 Dimerization Reactions; 2.2.3 Cycloaddition Reactions; References; 2.3 Other 1-Carbon Cumulenes; 2.3.1 Thiocarbonyl S-Imides; 2.3.2 Thiocarbonyl S-Sulfides; 2.3.3 1-Aza-2-azoniaallene Salts; References; 3 2-Carbon Cumulenes; 3.1 Carbon Oxides, O C O, :CO; 3.1.1 Introduction; 3.1.2 Cycloaddition Reactions 327 $a3.1.3 Insertion ReactionsReferences; 3.2 Carbon Sulfides, S C S, S CO; 3.2.1 Introduction; 3.2.2 Cycloaddition Reactions; 3.2.3 Insertion Reactions; References; 3.3 Carbon Nitrides; 3.3.1 Isocyanates, RN CO; References; 3.3.2 Isothiocyanates, RN C S; References; 3.3.3 Carbodiimides, RN C NR; References; 3.4 Center Carbon Phosphorallenes, P C P; 3.4.1 Introduction; 3.4.2 Dimerization Reactions; 3.4.3 Cycloaddition Reactions; References; 4 1,2-Dicarbon Cumulenes; 4.1 Ketenes, R2C C O; 4.1.1 Introduction; 4.1.2 Dimerization Reactions; 4.1.3 Trimerization Reactions; 4.1.4 Cycloaddition Reactions 327 $aReferences4.2 Thioketenes, R2C C S; 4.2.1 Introduction; 4.2.2 Dimerization Reactions; 4.2.3 Cycloaddition Reactions; References; 4.3 Ketenimines, R2C C NR; 4.3.1 Introduction; 4.3.2 Dimerization Reactions; 4.3.3 Cycloaddition Reactions; References; 4.4 1-Silaallenes, R2C C Si; 4.4.1 Introduction; 4.4.2 Dimerization Reactions; 4.4.3 Cycloaddition Reactions; References; 4.5 1-Phosphaallenes, R2C C P; 4.5.1 Introduction; 4.5.2 Dimerization Reactions; 4.5.3 Cycloaddition Reactions; References; 4.6 Other Metal Allenes; 4.6.1 Introduction; 4.6.2 Cycloaddition Reactions; References 327 $a5 1,3-Dicarbon Cumulenes5.1 Thiocarbonyl S-ylides, R2C S CH2; 5.2 2-Azaallenium Salts, R2C N+ CR2; 5.3 1-Oxa-3-azoniabutatriene Salts, R2C N+ C O; 5.4 1-Thia-3-azabutatriene Salts, R2C N+ C S; 5.5 Phosphorus Ylides; References; 6 1,2,3-Tricarbon Cumulenes; 6.1 Allenes, R2C C CR2; 6.1.1 Introduction; 6.1.2 Dimerization Reactions; 6.1.3 Oligomerization Reactions; 6.1.4 Cycloaddition Reactions; References; 6.2 [3] Cumulenes, R2C C C CR2; 6.2.1 Introduction; 6.2.2 Dimerization Reactions; 6.2.3 Trimerization Reactions; 6.2.4 Cycloaddition Reactions; References; 6.3 [4] Cumulenes, R2C C C C CR2 327 $a6.3.1 Introduction6.3.2 Dimerization Reactions; 6.3.3 Cycloaddition Reactions; References; 6.4 [5] Cumulenes, R2C C C C C CR2; 6.4.1 Introduction; 6.4.2 Dimerization Reactions; 6.4.3 Cycloaddition Reactions; References; 7 Noncarbon Cumulenes; 7.1 Azides, RN N N; 7.1.1 Introduction; 7.1.2 Oligomers; 7.1.3 [3+2] Cycloaddition Reactions; References; 7.1.4 Some Applications in Modifications of Biopolymers; Application References; 7.2 Triazaallenium Salts, RN N+ NR; 7.2.1 Introduction; 7.2.2 Cycloaddition Reactions; References; 7.3 Sulfur Oxides; 7.3.1 Introduction; 7.3.2 Sulfur Dioxide, O S O 327 $a7.3.3 Sulfur Trioxide, O SO2 330 $aCumulenes are organic molecules with two or more cumulative (consecutive) double bonds. Their reactions often proceed at room temperature, with or without a catalyst, and are stereospecific, giving the reaction products in high yields - features characteristic of "click reactions". Cumulenes in Click Reactions presents a comprehensive list of cumulene systems and their reactions, with an emphasis on their "click-like" nature. The chapters are structured according to the number of carbon atoms in the system, including coverage of: introduction to the chemist 606 $aAlkenes 606 $aChemical reactions 615 0$aAlkenes. 615 0$aChemical reactions. 676 $a547.2 676 $a547.412 700 $aUlrich$b Henri$f1925-$01658044 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911020332203321 996 $aCumulenes in click reactions$94417654 997 $aUNINA