00916nam0-22003011i-450 99000446469040332120210928101947.0000446469FED01000446469(Aleph)000446469FED0100044646919990530d1920----km-y0itay50------baitay-------001yyNote di guerraLuigi CapelloMilanoFratelli Treves19202 v.20 cm00100011291220011.: Dall'inizio alla presa di Gorizia00100011291320012.: Vodice - Bainsizza . Caporetto - la vittoria finaleCapello,Luigi136909ITUNINARICAUNIMARCBK9900044646904033214/ III F 10bibl.6869/3147FLFBC4/ III F 11bibl.7174/3465FLFBCFLFBCNote di guerra545188UNINA01196nam 2200349Ia 450 99639672830331620221108084804.0(CKB)4330000000330367(EEBO)2240956440(OCoLC)12219735(EXLCZ)99433000000033036719850701d1697 uy |engurbn#|||a|bb|A letter in answer to a book entitled, Christianity not mysterious[electronic resource] as also, to all those who set up for reason and evidence in opposition to revelation & mysteries /by Peter Browne ..Dublin Printed by Joseph Ray ... for John North ...1697[4], 231, [1] pErrata: p. [1] at end.Reproduction of original in British Library.eebo-0018DeismControversial literatureDeismBrowne Peterapproximately 1666-1735.1214978EAAEAAm/cUMIWaOLNBOOK996396728303316A letter in answer to a book entitled, Christianity not mysterious2806225UNISA01272nam a2200325 i 450099100350212970753620021217151710.0961025s1981 us a b 001 0 eng d0471035580b11821164-39ule_instLE00301925ExLDip.to Biologiaeng541.394Frost, Arthur Atwater17364Kinetics and mechanism /John W. Moore, Ralph G. Pearson3th ed. /John W. Moore, Ralph G. PearsonNew York :John Wiley & Sons,c1981xv, 455 p. :ill. ;24 cmRevision of: 2nd ed. / Arthur A. Frost, Ralph G. Pearson. 1961"A Wiley-Interscience publication"Includes bibliographical references and indexChemical reaction, Rate ofMoore, John W.Pearson, Ralph G.authorhttp://id.loc.gov/vocabulary/relators/aut16292.b1182116404-11-1018-12-02991003502129707536LE003 541.3 MOO01.01 (1981)12003000004090le003-E0.00-l- 01810.i1207165118-12-02Kinetics and mechanism129670UNISALENTOle00301-01-96ma -engus 0101314nas 2200373-a 450 991089141230332120240413015111.0(CKB)2560000000094790(CONSER)--2012273295(DE-599)ZDB2760788-4(EXLCZ)99256000000009479020060920a20049999 --- -engtxtrdacontentcrdamediacrrdacarrierDidactics of mathematicsWroclaw Publishing House of the Wroclaw University of Economics2004-1 online resourceRefereed/Peer-reviewedPrint version: Didactics of mathematics. 1733-7941 (DLC) 2012273295 (OCoLC)71367399 MathematicsStudy and teachingPeriodicalsMathématiquesÉtude et enseignementPériodiquesMathematicsStudy and teachingfast(OCoLC)fst01012236Periodicals.fastMathematicsStudy and teachingMathématiquesÉtude et enseignementMathematicsStudy and teaching.Uniwersytet Ekonomiczny we Wrocławiu.JOURNAL9910891412303321exl_impl conversionDidactics of mathematics4271423UNINA05263nam 2200673Ia 450 991102033220332120200520144314.09786612461071978128246107912824610799780470747957047074795197804707479330470747935(CKB)1000000000822301(EBL)470758(OCoLC)476311784(SSID)ssj0000336424(PQKBManifestationID)11229534(PQKBTitleCode)TC0000336424(PQKBWorkID)10281868(PQKB)10465452(MiAaPQ)EBC470758(Perlego)2756899(EXLCZ)99100000000082230120090827d2009 uy 0engur|n|---|||||txtccrCumulenes in click reactions /Henri UlrichHoboken, NJ Wiley20091 online resource (566 p.)Description based upon print version of record.9780470779323 0470779322 Includes bibliographical references and index.Cumulenes 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 Reactions3.1.3 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 ReactionsReferences4.2 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; References5 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 CR26.3.1 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 O7.3.3 Sulfur Trioxide, O SO2Cumulenes 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 chemistAlkenesChemical reactionsAlkenes.Chemical reactions.547.2547.412Ulrich Henri1925-1658044MiAaPQMiAaPQMiAaPQBOOK9911020332203321Cumulenes in click reactions4417654UNINA