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Volumn 10, Issue 21, 2008, Pages 5039-5042

Metal-free oxidative cyclization of urea-tethered alkenes with hypervalent iodine

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Indexed keywords


EID: 60949085100     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8022165     Document Type: Article
Times cited : (107)

References (31)
  • 1
    • 0042881024 scopus 로고    scopus 로고
    • Review
    • (a) Review: Müller, P.; Fruit, C. Chem. Rev. 2003, 103, 2905-2919.
    • (2003) Chem. Rev , vol.103 , pp. 2905-2919
    • Müller, P.1    Fruit, C.2
  • 10
    • 0036628555 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Zhdankin, V. V.; Stang, P. J. Chem. Rev. 2002, 102, 2523-2584.
    • (2002) Chem. Rev , vol.102 , pp. 2523-2584
    • Zhdankin, V.V.1    Stang, P.J.2
  • 27
    • 0000757366 scopus 로고    scopus 로고
    • 3 can be used in with iodine(III) reagents to generate the 1,2-diazide. (a) Moriarty, R. M.; Khosrowshahi, J. S. Tetrahedron Lett. 1986, 27, 2809-2812.
    • 3 can be used in with iodine(III) reagents to generate the 1,2-diazide. (a) Moriarty, R. M.; Khosrowshahi, J. S. Tetrahedron Lett. 1986, 27, 2809-2812.
  • 31
    • 54849415497 scopus 로고    scopus 로고
    • 4 to oxidatively cyclize tosylurea substrates appeared. Though the isourea products were isolated as byproducts from their reactions, in all cases the imidazolidinone (e.g., 3) was the major product. Muñiz, K.; Hövelmann, C. H.; Campos-Gómez, E.; Barluenga, J.; González, J. M.; Streuff, J.; Nieger, M. Chem. Asian J. 2008, 3, 776-788.
    • 4 to oxidatively cyclize tosylurea substrates appeared. Though the isourea products were isolated as byproducts from their reactions, in all cases the imidazolidinone (e.g., 3) was the major product. Muñiz, K.; Hövelmann, C. H.; Campos-Gómez, E.; Barluenga, J.; González, J. M.; Streuff, J.; Nieger, M. Chem. Asian J. 2008, 3, 776-788.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.