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Volumn 48, Issue 33, 2007, Pages 5751-5753

Efficient synthesis of 5- and 6-tributylstannylindoles and their reactivity with acid chlorides in the Stille coupling reaction

Author keywords

Acylation; Stille coupling reaction; Tributylstannylindole

Indexed keywords

5 TRIBUTYLSTANNYLINDOLE DERIVATIVE; 6 TRIBUTYLSTANNYLINDOLE DERIVATIVE; CHLORIDE; INDOLE DERIVATIVE; PALLADIUM; TIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34447521576     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.06.084     Document Type: Article
Times cited : (9)

References (23)
  • 20
    • 0001317382 scopus 로고
    • 5-Bromoindole is commercially available, 6-bromoindole was prepared by the Batcho-Leimgruber Indole synthesis from the 4-bromo-2-nitrotoluene in 62% overall yield, please see for references: and Ref. 4
    • 5-Bromoindole is commercially available, 6-bromoindole was prepared by the Batcho-Leimgruber Indole synthesis from the 4-bromo-2-nitrotoluene in 62% overall yield, please see for references:. Clarck R.D., and Repke D.B. Heterocycles 22 (1984) 195-221 and Ref. 4
    • (1984) Heterocycles , vol.22 , pp. 195-221
    • Clarck, R.D.1    Repke, D.B.2
  • 21
    • 34447556360 scopus 로고    scopus 로고
    • note
    • 33NSn: C, 59.14; H, 8.19; N, 3.45. Found: C, 59.39; H, 8.05; N, 3.58.
  • 23
    • 34447579621 scopus 로고    scopus 로고
    • note
    • 11NO: C, 77.81; H, 5.99; N, 7.56. Found: C, 78.03; H, 6.04; N, 7.47.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.