By Carroll Temple

Content material:
Chapter 1 Alkyl? or Aryl?Monosubstituted 1,2,4?Triazoles (pages 3–29):
Chapter 2 Alkyl? or Aryl?Disubstituted 1,2,4?Triazoles (pages 30–61):
Chapter three Alkyl? or Aryl?Trisubstituted 1,2,4?Triazoles (pages 62–95):
Chapter four 1,2,4?Triazolecarboxylic Acids and Their practical Derivatives (pages 96–120):
Chapter five Acyl?1,2,4?Triazoles (pages 121–129):
Chapter 6 Amino?1,2,4?Triazoles (pages 130–204):
Chapter 7 Diamino? and Triamino?1,2,4?Triazoles (pages 205–224):
Chapter eight Azido?, Azo?, Diazo?, Diazoamino (Triazeno?)?, Nitramino?, Nitrosamino?, and Nitro?1,2,4?Triazoles Containing a number of of those sensible teams (pages 225–238):
Chapter nine O?Substituted Oxy?1,2,4?Triazoles (pages 239–250):
Chapter 10 S?Substituted Thio?, Sulfinyl?, or Sulfonyl?1,2,4?Triazoles, 3,3??Dithobis[1,2,4?Triazoles], and 1,2,4?Triazolesulfonic Acids and Their practical Derivatives (pages 251–287):
Chapter eleven Mono?, Di?, and Trihalo?1,2,4?Triazoles (pages 288–296):
Chapter 12 1,2,4?Triazoles Containing a couple of consultant functionality (pages 297–364):
Chapter thirteen Alkyl or Aryl?1,2,4?Triazolin?5?Ones (pages 365–403):
Chapter 14 Alkyl? or Aryl?1,2,4?Triazoline?5?Thiones (pages 404–442):
Chapter 15 1,2,4?Triazolin?5?Ones Containing multiple consultant functionality (pages 443–474):
Chapter sixteen 1,2,4?Triazoline?5?thiones Containing a couple of consultant functionality (pages 475–502):
Chapter 17 Miscellaneous ?2(or ?1)?1,2,4?Triazolines Containing a number of consultant capabilities (pages 503–515):
Chapter 18 1,2,4?Triazolidines (pages 516–525):
Chapter 19 1,2,4?Triazolidine?3,5?diones (pages 526–558):
Chapter 20 1,2,4?Triazolidin?3?one?5?thiones and 1,2,4?Triazolidine?3,5?dithiones (pages 559–566):
Chapter 21 Bi?, Di, Bis?, Tris?, and Poly(1,2,4?Triazoles, Triazolines, and Triazolidines) associated both without delay or with Chain Containing Carbon (pages 567–598):
Chapter 22 1,2,4?Triazolium, Triazolinium, Triazolidinium, and Mesoionic Compounds (pages 599–658):
Chapter 23 Metal?triazole Complexes (pages 659–667):

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Additional info for Chemistry of Heterocyclic Compounds: Triazoles 1,2,4, Volume 37

Sample text

8-methyl-. 6-trimethylphenyf)- 72: P100713q. 82: P150485u 73: 4S42Sr 57: 39X2c 57: 3982a 57: 39X2a 7 6 PI 1 3 2 2 4 ~ 7 6 P113224p 7 2 i I007 I3q. 7 6 P113224p, 82: P1504XSu 6 5 1220Sa. 9645d, 73: 4S42Sr 72: P 1007 13q. 7 6 PI 1 3 2 2 4 ~ . 82: P15048Su 72: P100713q. 7 6 PI 1 3 2 2 4 ~ . 8 2 P1S0485u 5 4 2333e 72: 5 5 3 4 0 ~ 76: P113224p 68: 29646e, 57: 39X2a 72: P100713q. 7 6 P113224p. 82: PISO4XSu 7 6 PI 1 3 2 2 4 ~ 76 P 11 3 2 2 4 ~ 23: 836’. 53: 219041, 72: P100713q 76: PI 13224p 74 87901~ 5 4 2333c 7 6 PI 1 3 2 2 4 ~ 7 2 P100713q, 7 6 PI l3224p 72: P100713q, 7 6 113224~.

5-disubstituted triazoles. 2-6 (see Section 1 . ” In addition, other preformed triazoles have been used as intermediates. 1. ” References 1. 4 9 11630g 5 . 57: 3982a 9. 83: 28165 2. 46: lll47a 6. 51: 12079a 3. 47: 4335a I . 67:43155e 4. 69 35596a 8. 3. 3,4-A&yl- or Aryl-Disubstituted 4H-1,2,4-Triazoles Several methods have been developed for the preparation of 3,4disubstituted triazoles by intermolecular cyclization of two reactants. 3. ' Although the products are obtained in good yields, the formation of two types of by-products was observed.

3-23 37 23-24 nervous system agents. These benzodiazepines are prepared from 442benzoylpheny1)triazole intermediates," and a number of reports have appeared on the preparation of the latter. '* The type of compound has also been prepared by periodate oxidation of s-triazolo[4,3-a Jquin~lines'"~'~ and clucoph HO ~ 2 ~"1 . 3-30 References I. 66~46412h 5. 71: 706071 9. 74: 12557Ye 13. 77: 1 2 6 7 0 7 ~ 17. 73: 66S17n 21. 74: lllY68u 2. 62: 1647a f'136354rn 88SS7k 126708~ 2964Sd 3. 7. 1I. 15: 6. 7 8 10.

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