SCOPUS 정보 검색 플랫폼

Volumn 31, Issue 47, 1990, Pages 6757-6758

Iodopyridines from bromo- and chloropyridines

Author keywords

[No Author keywords available]

Indexed keywords

PYRIDINE DERIVATIVE;

ARTICLE; METHODOLOGY; NONHUMAN; PRIORITY JOURNAL; SYNTHESIS;

EID: 0025168806 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)97163-6 Document Type: Article

Times cited : (36)

References (15)

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- Newkome¹ Roper²

2
- 84985659387
- Palladium-Catalyzed Coupling Reaction ofN-Heteroaryl Halides with Functionalized Alkylzinc Iodides
- (1988) Synthesis , pp. 485
- Sakamoto¹ Nishimura² Kondo³ Yamanaka⁴

4
- 84867614766
- �ber die Quecksilberverbindungen des 4-Aminopyridins
- (1959) Journal f�r Praktische Chemie , vol.8 , pp. 156
- Profft¹ Otto²

6
- 85008061075
- Studies on organometallic compounds. II. Facile and convenient method for the synthesis of iodoazines through iododestannation of trimethylstannylazines.
- (1982) CHEMICAL & PHARMACEUTICAL BULLETIN , vol.30 , pp. 1731
- Yamamoto¹ Yanagi²

7
- 0002970352
- and references therein
- (1986) J. Org. Chem. , vol.51 , pp. 953
- Newkome¹ Moorfield² Sabbaghian³

8
- 84918600911
- Chem. Abstr. 45 1945 8525i
- (1945) J. Pharm. Soc. Japan , vol.65 , pp. 70
- Itai¹

9
- 33745658006
- (1965) Adv. Heterocycl. Chem. , vol.4 , pp. 146
- Shepherd¹ Fedrick²

10
- 37049106282
- 4-Dialkylaminopyridines: super acylation and alkylation catalysts
- For a review, see
- (1983) Chemical Society Reviews , pp. 129
- Scriven¹

11
- 5644266828
- 5 at 25°
- (1954) Z. Physik. Chem. , vol.202 , pp. 474
- Pavlopoulos¹ Strehlow²

12
- 37049054341
- 859. The hydrolysis of acetic anhydride. Part VII. Catalysis by pyridine and methylpyridines in acetate buffers
- The same explanation has been advanced to explain the lack of activity of 2-methylpyridine as an acylation catalyst;
- (1961) Journal of the Chemical Society (Resumed) , pp. 4362
- Butler¹ Gold²

14
- 84918653170
- The reactions are best followed by GC of a worked-up aliquot, as the starting material and products are generally not separated by silica gel TLC. In some instances, the reaction appears to stop after 5–6 hours; addition of a further equivalent of AcCl and NaI usually drives the reaction to completion.

15
- 58949096871
- 4
- (1915) J. Russ. Phys. Chem. Soc. , vol.46 , pp. 1571
- Chichihabin¹ Rjazancev²

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