ライフサイエンスコーパス: diazotization

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1 ve been synthesized from stable complexes by diazotization and azo-compound formation.

2 cotinic acid by selective reduction and then diazotization, and from N-(6-chloropyridin-3-ylmethyl)mo

3 loaddition, insertion of SO2 , 1,4-addition, diazotization, and tautomerization.

4 A diazotization/azide reaction sequence was used to conver

5 s by a variety of different methods, such as diazotization, Bamford-Stevens-type elimination, and dia

6 Thus, the ATMS/diazotization chemistry facilitated covalent binding of

7 ation analyses of microarrays made with ATMS/diazotization chemistry showed very sensitive detection

8 ng the p-aminophenyl trimethoxysilane (ATMS)/diazotization chemistry that was developed, microarrays

9 The nonaqueous diazotization/chloro dediazoniation (acetyl chloride/ben

10 Nonaqueous diazotization-dediazoniation of two types of aminopurine

11 ne cyclopentanol 14, has been developed from diazotization, elimination, stereoselective epoxidation,

12 essive cyclization with cyanogen bromide and diazotization in the presence of an appropriate cupric h

13 The first, shown in Scheme 1, involves diazotization/iodination of the corresponding aminofluor

14 erocycle isoguanine is prepared by selective diazotization of 2,6-diaminopurine and then converted to

15 ylbenzyne, has been prepared in low yield by diazotization of 3,4,5,6-tetraphenylanthranilic acid, an

16 Diazotization of 3d under anhydrous conditions with TFA/

17 arbonitrile (28) and methyl isocyanate or by diazotization of 5-amino-1-(N-methylcarbamoyl)imidazole-

18 Additionally, the in situ diazotization of a number of anilines allows the directi

19 lly substituted benzyne intermediates by the diazotization of anthranilic acids in the presence of Ba

20 by reduction of the nitro groups followed by diazotization of the amines.

21 Diazotization of the aniline into an aryl diazonium, usi

22 aniline derivative 13 followed by selective diazotization of the arylamine.

23 timized procedures enable sequential aniline diazotization/palladium-catalyzed Heck-Matsuda reaction

24 ia the 2-amino intermediate (3) using a mild diazotization procedure.

25 The method is based on the diazotization reaction of dapsone (4,4'-diamino-diphenyl

26 of phenyl and aminophenyl (Ph-PhNH2/GCE) by diazotization reaction.

27 nitrobenzimidazole (11) into iodo groups via diazotization reactions.

28 ) via successive reduction, cyclization, and diazotization reactions.

29 butyl nitrite (TBN) or sodium nitrite as the diazotization reagent.

30 be effected starting with ArNH(2) by in situ diazotization with [NO][BF(4)] followed by reaction with

31 rted to the O(6)-allyl derivatives that upon diazotization with t-BuONO and TMS-N(3) yield the C-2 az

32 a more reactive bromine atom via nonaqueous diazotization with tert-butyl nitrite, and the resultant

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