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Volumn 15, Issue 16, 2013, Pages 4218-4221

Nitro-methyl redox coupling: Efficient approach to 2-hetarylbenzothiazoles from 2-halonitroarene, methylhetarene, and elemental sulfur

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EID: 84882757438     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol401944a     Document Type: Article
Times cited : (106)

References (35)
  • 26
    • 84859581673 scopus 로고    scopus 로고
    • For a recent example using elemental sulfur as the sulfur synthon in the synthesis of benzothiazoles from aldehydes and 2-iodoanilines, see: Deng, H.; Li, Z.; Ke, F.; Zhou, X. Chem.-Eur. J. 2012, 18, 4840
    • (2012) Chem.-Eur. J. , vol.18 , pp. 4840
    • Deng, H.1    Li, Z.2    Ke, F.3    Zhou, X.4
  • 30
    • 0001443356 scopus 로고
    • 3 was observed under more drastic thermal uncatalyzed conditions when a solution of sulfur in 4-picoline (bp 145 C) was refluxed: Thayer, H. I.; Corson, B. B. J. Am. Chem. Soc. 1948, 70, 2330
    • (1948) J. Am. Chem. Soc. , vol.70 , pp. 2330
    • Thayer, H.I.1    Corson, B.B.2
  • 31
    • 33947478527 scopus 로고
    • The formation of di-(4-picolyl) and related compounds via a radical mechanism: Pryor, W. A. J. Am. Chem. Soc. 1960, 82, 2715
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 2715
    • Pryor, W.A.1
  • 33
    • 84882766189 scopus 로고
    • When nitrobenzene was heated at 120 C for 24 h with sulfur in 4-picoline, thioisonicotinanilide (25%) was obtained. This observation is in agreement with the literature report: Emmertt, B.; Holz, A. Chem. Ber. 1954, 676
    • (1954) Chem. Ber. , pp. 676
    • Emmertt, B.1    Holz, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.