LEADER 00806nam a2200253 i 4500 001 991003245259707536 005 20020503185401.0 008 001103s1966 it ||| | ita 035 $ab10478383-39ule_inst 035 $aEXGIL117585$9ExL 040 $aBiblioteca Interfacoltà$bita 082 0 $a851.1 100 1 $aPanziera, Ugo$0258206 245 13$aLe laudi /$cUgo Panziera 250 $a4. ed 260 $aRoma :$bEdizioni Paoline,$c1966 300 $a145 p. ;$c17 cm. 490 0 $aMaestri ;$v172 907 $a.b10478383$b21-02-17$c27-06-02 912 $a991003245259707536 945 $aLE002 Lett. I L 37$g1$i2002000502339$lle002$o-$pE0.00$q-$rl$s- $t0$u0$v0$w0$x0$y.i10552406$z27-06-02 996 $aLaudi$9213761 997 $aUNISALENTO 998 $ale002$b01-01-00$cm$da $e-$fita$git $h3$i1 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