LEADER 01283nam0-22003011i-450- 001 990000114020403321 035 $a000011402 035 $aFED01000011402 035 $a(Aleph)000011402FED01 035 $a000011402 100 $a20011111d--------km-y0itay50------ba 101 0 $aita 105 $ay-------001yy 200 1 $aStresa '84.'85$econferenza del traffico e della circolazione$e3-5 ottobre 1984$e40. conferenza$eil piano nazionale deitrasporti, implicazioni e riflessi sull'economia e sull'utenza automobilistica prezzi controllati e prezzi ammnistrati dei carburanti$g2-4 ottobre 1985$e41. conferenza$ela sicurezza stradale , una politica unitaria dei trasporti , le prospettive dopo il piano generale. 210 $aMilano$cAutomobil club di Milano$dcopyr. 1985 215 $a208 p.$cill.$d30 cm 300 $aLe notizie relative all'area del tit. sono ricavate dalla cop. 610 0 $aCircolazione stradale$aCongressi$a1984$a1985 676 $a629.04 710 12$aCONFERENZA DEL TRAFFICO E DELLA CIRCOLAZIONE, 40.-41., Stresa, 1984-1985$0333285 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990000114020403321 952 $a13 G 07 27$b6188$fFINBC 959 $aFINBC 996 $aStresa '84.'85$9115230 997 $aUNINA DB $aING01 LEADER 01090nam a22002651i 4500 001 991001145699707536 005 20021127162657.0 008 021123s1978 it |||||||||||||||||ita 035 $ab12106124-39ule_inst 035 $aARCHE-019592$9ExL 040 $aDip.to Filologia Ling. e Lett.$bita$cA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l. 100 1 $aTasso, Torquato$0294660 245 10$aLettere /$cTorquato Tasso ; a cura di Ettore Mazzali 260 $aTorino :$bEinaudi,$c[1978] 300 $a2 v. (XIII, 449 p. compless.) ;$c20 cm 490 0 $aClassici Ricciardi ;$v75 650 4$aTasso, Torquato$xLettere e carteggi 700 1 $aMazzali, Ettore 907 $a.b12106124$b28-04-17$c01-04-03 912 $a991001145699707536 945 $aLE008 TS D III 8/I$cV. 1$g1$i2008000383213$lle008$o-$pE0.00$q-$rl$s- $t0$u0$v0$w0$x0$y.i12410445$z01-04-03 945 $aLE008 TS D III 8/II$cV. 2$g1$i2008000383220$lle008$o-$pE0.00$q-$rl$s- $t0$u0$v0$w0$x0$y.i12410457$z01-04-03 996 $aLettere$9150583 997 $aUNISALENTO 998 $ale008$b01-04-03$cm$da $e-$fita$git $h0$i2 LEADER 05191nam 2200625 450 001 9910831161403321 005 20230422044832.0 010 $a1-281-84252-4 010 $a9786611842529 010 $a3-527-61406-0 010 $a3-527-61407-9 035 $a(CKB)1000000000376618 035 $a(EBL)481969 035 $a(OCoLC)291092539 035 $a(SSID)ssj0000201627 035 $a(PQKBManifestationID)11196343 035 $a(PQKBTitleCode)TC0000201627 035 $a(PQKBWorkID)10245717 035 $a(PQKB)11131036 035 $a(MiAaPQ)EBC481969 035 $a(EXLCZ)991000000000376618 100 $a20160820h19991999 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aMetal carbenes in organic synthesis /$fFlorencio Zaragoza Do?rwald 210 1$aWeinheim, [Germany] :$cWiley-VCH,$d1999. 210 4$d©1999 215 $a1 online resource (311 p.) 300 $aDescription based upon print version of record. 311 $a3-527-29625-5 320 $aIncludes bibliographical references and index. 327 $aMetal Carbenes in Organic Synthesis; Table of Contents; Abbreviations; Experimental Procedures; 1 The Carbon-Metal Double Bond; 1 1 Reactivity of Carbene Complexes; 1.2 Fischer-Type and Schrock-Type Carbene Complexes: Theoretical Treatment; 1.3 Olefin Metathesis and Olefin Cyclopropanation; 1.4 Characteristic NMR Data; 2 Heteroatom-Substituted Carbene Complexes; 2.1 Generation of Heteroatom-Substituted Carbene Complexes; 2.1.1 From Acyl Complexes; 2.1.1.1 From Acyl Complexes Generated from Carbonyl Complexes; 2.1.1.2 From Acyl Complexes Generated from Metallates 327 $a2.1.1.3 From Acyl Complexes Generated by Other Methods2.1.2 From Isonitrile Complexes; 2.1.3 From a-Haloiminium Salts and Metallates; 2.1.4 From Carboxamides and Metallates; 2.1.5 From Vinylidene Complexes; 2.1.5.1 From Vinylidene Complexes Generated from Alkynes; 2.1.5.2 From Vinylidene Complexes Generated from Alkynyl Complexes; 2.1.6 From Carbenes and Carbenoids; 2.1.7 From Alkyl Complexes by a-Abstraction; 2.1.8 From Carbyne Complexes; 2.1.9 Other Methods; 2.2 Synthetic Applications of Heteroatom-Substituted Carbene Complexes; 2.2.1 General Considerations 327 $a2.2.2 Demetallation and Formation of Acyclic Products2.2.3 Photochemical Transformations; 2.2.4 Cyclopropanation; 2.2.5 Thermal Benzannulations; 2.2.5.1 The Do?tz Benzannulation Reaction; 2.2.5.2 Other Thermal Benzannulations; 2.2.6 Formation of Five-Membered Rings; 2.2.6.1 Cyclization of (1,3-Butadien-1-yl)carbene Complexes; 2.2.6.2 Cyclization of Functionalized Carbene Complexes; 2.2.6.3 Rearrangement of Ammonium Ylides; 2.2.6.4 Other Methods; 2.2.7 Formation of Six-Membered. Non-Aromatic Carbocycles and Six-Membered Heterocycles; 2.2.8 Formation of Seven-Membered Rings 327 $a3 Non-Heteroatom-Substituted Carbene Complexes3.1 Generation of Non-Heteroatom-Substituted Carbene Complexes; 3.1.1 a-Abstraction of Electrophiles (Nucleophilic Abstraction); 3.1.2 a-Abstraction of Nucleophiles (Electrophilic Abstraction); 3.1.2.1 a-Abstraction of Hydride; 3.1.2.2 a-Abstraction of Oxygen-Bound Leaving Groups; 3.1.2.3 a-Abstraction of Thioethers; 3.1.2.4 a-Abstraction of Halides; 3.1.3 From Ylides; 3.1.3.1 From Diazoalkanes; 3.1.3.2 From Other Ylides; 3.1.4 From Carbyne Complexes; 3.1.4.1 Nucleophilic Additions to Carbyne Complexes 327 $a3.1.4.2 Electrophilic Additions to Carbyne Complexes3.1.5 From Alkynyl and Alkenyl Complexes; 3.1.6 From Alkyne and Cyclopropene Complexes; 3.1.7 By [2 + 2] Cycloreversion; 3.1.8 Other Methods; 3.2 Synthetic Applications of Non-Heteroatom-Substituted Carbene Complexes; 3.2.1 General Considerations; 3.2.2 Cyclopropanation; 3.2.2.1 Stoichiometric Cyclopropanations; 3.2.2.2 Catalytic Cyclopropanations with Diazoalkanes; 3.2.2.3 Catalytic Cyclopropanations with Other Carbene Precursors; 3.2.3 C-H Insertions; 3.2.3.1 C-H Insertions of Nucleophilic Carbene Complexes 327 $a3.2.3.2 C-H Insertions of Electrophilic Carbene Complexes 330 $aThere are hardly more versatile compounds in organic synthesis than carbene complexes. The rapid development of new synthetic methods involving carbene complexes - stereoselective cyclopropanation, carbonyl olefination, olefin metathesis, etc. - reveals the value and high potential of these compounds. Their application ranges from the synthesis of fine chemicals to polymer production.This comprehensive, well structured handbook presents the fundamental principles and the recent advances in carbene complex chemistry. Arranged according to structure and reactivity, all relevant classes 606 $aCarbenes (Methylene compounds) 606 $aOrganic compounds$xSynthesis 615 0$aCarbenes (Methylene compounds) 615 0$aOrganic compounds$xSynthesis. 676 $a547.050459 676 $a547.2 700 $aDo?rwald$b Florencio Zaragoza$0875082 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910831161403321 996 $aMetal carbenes in organic synthesis$92004808 997 $aUNINA