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Volumn 350, Issue 9, 2008, Pages 1355-1359

Reactivity of electrogenerated N-heterocyclic carbenes in room-temperature ionic liquids. Cyclization to 2-azetidinone ring via C-3/C-4 bond formation

Author keywords

lactams; Carbenes; Cyclization; Electrochemistry; Imidazolium based RTILs

Indexed keywords


EID: 50249101313     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200800049     Document Type: Article
Times cited : (54)

References (58)
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    • and references cited therein; Concerning the use of N-heterocyclic carbenes in organic synthesis, see
    • a) Concerning the use of N-heterocyclic carbenes in organic synthesis, see: D. Enders, O. Niemeier, A. Henseler, Chem. Rev. 2007, 107, 5606-5655, and references cited therein;
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    • Recently, a carbene-catalyzed Staudinger reaction in molecular solvent (THF) has been reported. The carbene was generated from suitable precursors with t-BuOK in THF: Y.-R. Zhang, L. He, X. Wu, P.-L. Shao, S. Ye, Org. Lett. 2008, 10, 277-280.
    • b) Recently, a carbene-catalyzed Staudinger reaction in molecular solvent (THF) has been reported. The carbene was generated from suitable precursors with t-BuOK in THF: Y.-R. Zhang, L. He, X. Wu, P.-L. Shao, S. Ye, Org. Lett. 2008, 10, 277-280.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.