Detailed table of contents (pdf)

More documents

Recommendations

Info

XXX Table of Contents 17.2.2.1.5.1.3.1.4 Variation 4: Reactions of 3-(Methylsulfonyl)-1,2,4-triazines with Nucleophiles .............................................. 405 17.2.2.1.5.1.3.1.5 Variation 5: Reactions of 3-(Alkylsulfanyl)-1,2,4-triazines with Nucleophiles .............................................. 405 17.2.2.1.5.1.3.2 Method 2: Suzuki Coupling Reactions with 3-(Alklylsulfanyl)-1,2,4-triazines ............................ 406 17.2.2.1.5.1.3.3 Method 3: By Diazotization .......................................... 407 17.2.2.1.5.2 Addition Reactions ....................................................... 407 17.2.2.1.5.2.1 Method 1: Synthesis of 1,2,4-Triazine N-Oxides from 1,2,4-Triazines .... 407 17.2.2.1.5.2.2 Method 2: Alkylation of 1,2,4-Triazine N-Oxides ....................... 408 17.2.2.1.5.3 Modification of Substituents .............................................. 409 17.2.2.1.5.3.1 Method 1: C—C Bond Formation at a Methyl Group .................... 409 17.2.2.1.5.3.2 Method 2: Oxidation of 3-Hydrazino-1,2,4-triazine 1-Oxides ........... 409 17.2.2.2 1,2,4-Benzotriazines and Related Compounds .............................. 410 17.2.2.2.1 Synthesis by Ring-Closure Reactions ....................................... 410 17.2.2.2.1.1 By Formation of One N—N and One N—C Bond ............................. 410 17.2.2.2.1.1.1 Fragments N—C—C—N and N—C ........................................... 410 17.2.2.2.1.1.1.1 Method 1: Reaction of 2-Nitroaniline with Cyanamide ................. 410 17.2.2.2.1.1.2 Fragments N—C—N and N—C—C ........................................... 411 17.2.2.2.1.1.2.1 Method 1: Reactions of 2-Nitroarenes with Guanidines ................ 411 17.2.2.2.1.1.2.2 Method 2: Reactions of Nitronaphthalenes with Guanidine ............. 412 17.2.2.2.1.1.3 Fragments N—C—N—C—C and N ........................................... 413 17.2.2.2.1.1.3.1 Method 1: Reactions of Arylbenzamidoximes with Nitrile Oxides ....... 413 17.2.2.2.1.2 By Formation of Two N—C Bonds .......................................... 414 17.2.2.2.1.2.1 Fragments N—N—C—N and C—C ........................................... 414 17.2.2.2.1.2.1.1 Method 1: Reactions of Cycloalkane-1,2-diones with Amidrazones ..... 414 17.2.2.2.1.2.1.2 Method 2: Cycloaddition of N-(Phenylmethylene)aniline and Diethyl Azodicarboxylate .................................. 415 17.2.2.2.1.2.2 Fragments N—N—C and N—C—C ........................................... 415 17.2.2.2.1.2.2.1 Method 1: Reactions of 6-Nitroquinoline with Aldehyde Hydrazones .... 415 17.2.2.2.1.2.3 Fragments N—C—C—N—N and C ........................................... 416 17.2.2.2.1.2.3.1 Method 1: Cyclization of 3,4-Dihydronaphthalene-1,2-dione 1-Hydrazone 2-Oxime with Ortho Esters ................... 416 17.2.2.2.1.3 By Formation of One N—N Bond ........................................... 417 17.2.2.2.1.3.1 Fragment N—C—N—C—C—N ............................................... 417 17.2.2.2.1.3.1.1 Method 1: Cyclization of (2-Nitronaphthyl)thioureas ................... 417 17.2.2.2.1.3.1.1.1 Variation 1: Cyclization of 2-(2-Nitrophenyl)pyrazol-3-amines ........... 417 17.2.2.2.1.4 By Formation of One N—C Bond ........................................... 418 17.2.2.2.1.4.1 Fragment N—N—C—N—C—C ............................................... 418
Table of Contents XXXI 17.2.2.2.1.4.1.1 Method 1: Oxidation of N-Phenylsulfonylbenzamidrazones ............. 418 17.2.2.2.1.4.1.2 Method 2: Cyclization of N 1 -Isopropylidene-N 3 -arylamidrazones ........ 419 17.2.2.2.1.4.2 Fragment C—C—N—N—C—N ............................................... 419 17.2.2.2.1.4.2.1 Method 1: Reactions of 1,2-Dicarbonyl Compounds with Amidrazones and Related Compounds .................................. 420 17.2.2.2.1.4.2.2 Method 2: Cyclization of Formazans .................................. 420 17.2.2.2.1.4.3 Fragment N—C—C—N—N—C ............................................... 421 17.2.2.2.1.4.3.1 Method 1: Cyclization of 1-(2-Nitrophenyl)-2-[nitro(phenyl)methylene]hydrazines ................................................ 422 17.2.2.2.1.4.3.1.1 Variation 1: Cyclization of N-(2-Nitrophenyl)benzenecarbohydrazonoyl Bromide .................................................. 422 17.2.2.2.1.4.3.1.2 Variation 2: Cyclization of (2-Nitrophenyl)hydrazones ................... 423 17.2.2.2.1.2.3.2 Method 2: Cyclization of N¢-(2-Aminophenyl)acetohydrazide ........... 424 17.2.2.2.1.2.3.2.1 Variation 1: Cyclization of Ethyl 2-(2-aminophenyl)hydrazinecarboxylate . 424 17.2.2.2.2 Annulation by Formation of a Benzenoid Ring .............................. 425 17.2.2.2.2.1 Method 1: Cycloaddition of 5,6-Bis(bromomethylene)-1,2,4-triazine with a Dieneophile ........................................ 425 17.2.2.2.2.2 Method 2: Photocyclization of 1-Methyl-3,5,6-triphenyl-1,2,4-triazinium Iodide .................................................... 426 17.2.2.2.3 Synthesis by Ring Transformation .......................................... 426 17.2.2.2.3.1 Method 1: Cyclization of 3-(2-Acylaminophenyl)sydnones with Hydrogen Cyanide ........................................ 426 17.2.2.2.3.2 Method 2: Ring Enlargement of 2,1,3-Benzoxadiazole 1-Oxide with Diethylamine ............................................. 427 17.2.2.2.3.3 Method 3: Reactions of [1,2,5]-Oxadiazolo[3,4-b]quinoxaline 1-Oxides with Nitrile Oxides ........................................ 427 17.2.2.2.3.4 Method 4: Ring Scission of N¢-[2-(1H-1,2,3-Benzotriazol-1-yl)ethylidene]- 4-methylbenzenesulfonohydrazides ........................ 428 17.2.2.2.3.5 Method 5: Flash-Vacuum Pyrolysis of a-(1-Benzotriazolyl)-boxotributylphosphorus Ylides .............................. 428 17.2.2.2.3.6 Method 6: Oxidation of Benzimidazole-1,2-diamines .................. 429 17.2.2.2.3.7 Method 7: Oxidation of 1-Amino-2-quinoxalones ...................... 429 17.2.2.2.4 Aromatization ............................................................ 430 17.2.2.2.4.1 Method 1: By Oxidation of 1,2-Dihydro-1,2,4-benzotriazines ........... 430 17.2.2.2.4.2 Method 2: Aromatization of 5,6,7,8-Tetrahydro-1,2,4-benzothiazines ... 430 17.2.2.2.4.3 Method 3: Conversion of 1,2,4-Benzotriazinones into 3-Halo-1,2,4benzotriazines ............................................ 430 17.2.2.2.5 Synthesis by Substituent Modification ..................................... 431 17.2.2.2.5.1 Substitution of Existing Substituents ....................................... 431 17.2.2.2.5.1.1 Of Carbon .......................................................... 431 17.2.2.2.5.1.2 Of Heteroatoms .......................................................... 432 17.2.2.2.5.1.2.1 Method 1: Substitution of Halogens .................................. 432 17.2.2.2.5.1.2.2 Method 2: Deoxygenation of N-Oxides ................................ 433
Page 1 and 2: Table of Contents IX Volume 17: Six
Page 3 and 4: Table of Contents XI Table of Conte
Page 5 and 6: Table of Contents XIII 17.1.1.2.4.1
Page 7 and 8: Table of Contents XV 17.1.2.3.1.3 B
Page 9 and 10: Table of Contents XVII 17.1.3.2 1,4
Page 11 and 12: Table of Contents XIX 17.1.3.3.1.1.
Page 13 and 14: Table of Contents XXI 17.2 Product
Page 15 and 16: Table of Contents XXIII 17.2.1.2.1.
Page 17 and 18: Table of Contents XXV 17.2.1.3.1.1
Page 19 and 20: Table of Contents XXVII 17.2.2 Prod
Page 21: Table of Contents XXIX 17.2.2.1.3.3
Page 25 and 26: Table of Contents XXXIII 17.2.3.1.1
Page 27 and 28: Table of Contents XXXV 17.2.3.1.2.2
Page 29 and 30: Table of Contents XXXVII 17.2.3.1.4
Page 31 and 32: Table of Contents XXXIX 17.3.3.2 Sy
Page 33 and 34: Table of Contents XLI 17.4.2.2.2.2
Page 35 and 36: Table of Contents XLIII 17.4.4.1.2.
Page 37 and 38: Table of Contents XLV 17.4.5.1.2.3
Page 39 and 40: Table of Contents XLVII 17.4.5.4.1.
Page 41 and 42: Table of Contents XLIX 17.4.6.2.4.2
Page 43 and 44: Table of Contents LI 17.4.6.5.4.2 A
Page 45 and 46: Table of Contents LIII 17.4.6.7.4.4
Page 47 and 48: Table of Contents LV 17.5.2.2.1 Met
Page 49 and 50: Table of Contents LVII 17.6.2.1.1.4
Page 51 and 52: Table of Contents LIX 17.6.5.2.2.1.
Page 53 and 54: Table of Contents LXI 17.7.3.2 [2.3
Page 55 and 56: Table of Contents LXIII 17.7.5.1.2.
Page 57 and 58: Table of Contents LXV 17.8.3.2 Cont
Page 59 and 60: Table of Contents LXVII 17.9.8.3 Me
Page 61: Table of Contents LXIX 17.9.22.3 Me

Detailed table of contents (pdf)

Create successful ePaper yourself

Delete template?

Save as template?