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Volumn 47, Issue 37, 2006, Pages 6505-6507

Oxidative synthesis of azacyclic derivatives through the nitrenium ion: application of a hypervalent iodine species electrochemically generated from iodobenzene

Author keywords

Anodic oxidation; Azaspiro 4.5 decane; Hypervalent iodine; Quinolinone

Indexed keywords

QUINOLINE DERIVATIVE;

EID: 33746855837     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.07.050     Document Type: Article
Times cited : (72)

References (19)
  • 5
    • 85007767664 scopus 로고
    • (review in Japanese)
    • (review in Japanese). Kikugawa Y. J. Syn. Org. Chem. 48 (1990) 749-757
    • (1990) J. Syn. Org. Chem. , vol.48 , pp. 749-757
    • Kikugawa, Y.1
  • 14
    • 33746858238 scopus 로고    scopus 로고
    • note
    • 2O, and extracted with EtOAc. The organic layer was dried and evaporated. The residue was chromatographed on preparative TLC to give 2a in quantitative yield. Upon using 1.5 equiv mol of iodobenzene, the desired 2a was obtained in 90% yield, whereas 1.2 equiv mol of iodobenzene provided the product in 50% yield.
  • 19
    • 33746853195 scopus 로고    scopus 로고
    • Application of this method to oxidation of mangostin derivatives provided a regioselective oxidation, which was not observed by PIFA: Nishihama, Y.; Amano, Y.; Ogamino, T.; Nishiyama, S. Electrochemistry, in press.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.