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Volumn 55, Issue 3, 2014, Pages 694-698

ZnCl2 promoted efficient, one-pot synthesis of 3-arylmethyl and diarylmethyl indoles

Author keywords

3 Diarylmethyl indole; Friedel Crafts reaction; Multicomponent reaction; Pressure tube reaction; Zinc chloride

Indexed keywords

3 ARYLMETHYL INDOLE DERIVATIVE; BIS(INDOLYL)METHANE; DIARYLMETHYL INDOLE DERIVATIVE; INDOLE DERIVATIVE; METHANE; UNCLASSIFIED DRUG; ZINC CHLORIDE;

EID: 84891830850     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.11.115     Document Type: Article
Times cited : (35)

References (36)
  • 1
    • 84862291173 scopus 로고    scopus 로고
    • references cited therein
    • M. Shiri Chem. Rev. 112 2012 3508 3549 and references cited therein
    • (2012) Chem. Rev. , vol.112 , pp. 3508-3549
    • Shiri, M.1
  • 36
    • 84891828987 scopus 로고    scopus 로고
    • 2), 5.59 (1H, s, Ar-CH), 6.58-6.59 (1H, m, ArH), 6.68
    • 2 (136 mg, 1 mmol) or (b) anhydrous aluminum chloride (133 mg, 1 mmol) were successively added and heated in the oil bath at 140 C for 5 h. The product was isolated from the reaction mixture as stated in 3-diarylmethyl indole synthesis above. (a) Yield = 176 mg (54%) (b) Yield = 232 mg (71%).
    • Representative Procedure for 3-diarylmethyl Indole Synthesis


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.