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Volumn 53, Issue 40, 2012, Pages 5426-5429

A furoindoline synthesis by remote radical functionalization

Author keywords

Furoindoline; Heterocycle; Indoline; Radical; Remote functionalization

Indexed keywords

CHOLINERGIC RECEPTOR BLOCKING AGENT; FUROINDOLINE; HYDROGEN; PHENYL GROUP; TERTIARY AMINE; UNCLASSIFIED DRUG;

EID: 84865690805     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.07.115     Document Type: Article
Times cited : (9)

References (48)
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    • An interrupted Fischer reaction generates intermediates 2 directly from phenylhydrazines and lactols, see
    • An interrupted Fischer reaction generates intermediates 2 directly from phenylhydrazines and lactols, see: B.W. Boal, A.W. Schammel, and N.K. Garg Org. Lett. 11 2009 3458
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  • 23
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    • For examples of complementary routes that do not rely on the classical cyclizations outlined in Scheme 1, see
    • For examples of complementary routes that do not rely on the classical cyclizations outlined in Scheme 1, see: Y. Liu, W. Xu, and X. Wang Org. Lett. 12 2010 1448
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    • Liu, Y.1    Xu, W.2    Wang, X.3
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    • Outside of the context of furoindoline synthesis, the cyclization of an oxygen nucleophile onto a carbon atom adjacent to nitrogen is typically achieved by amine→imine oxidation and subsequent nucleophilic attack. For representative examples, see
    • Outside of the context of furoindoline synthesis, the cyclization of an oxygen nucleophile onto a carbon atom adjacent to nitrogen is typically achieved by amine→imine oxidation and subsequent nucleophilic attack. For representative examples, see: C.-K. Chen, A.G. Hortmann, and M.R. Marzabadi J. Am. Chem. Soc. 110 1988 4829
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 4829
    • Chen, C.-K.1    Hortmann, A.G.2    Marzabadi, M.R.3
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    • The synthesis of spiroaminals by 1,5- or 1,6-HAT is restricted to the cyclization of an amine nucleophile onto a cation resonance stabilized by oxygen, see
    • J. Sperry, Y.-C. Liu, and M.A. Brimble Org. Biomol. Chem. 8 2010 29 The synthesis of spiroaminals by 1,5- or 1,6-HAT is restricted to the cyclization of an amine nucleophile onto a cation resonance stabilized by oxygen, see
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 29
    • Sperry, J.1    Liu, Y.-C.2    Brimble, M.A.3
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    • references therein
    • M. Koag, and S. Lee Org. Lett. 13 2011 4766 and references therein
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    • For an example of related 1,5-HAT under reductive conditions, see:, (see Table 2, compound 1i)
    • For an example of related 1,5-HAT under reductive conditions, see: H. Zhu, J.G. Wickenden, N.E. Campbell, J.C.T. Leung, K.M. Johnson, and G.M. Sammis Org. Lett. 11 2009 2019 (see Table 2, compound 1i)
    • (2009) Org. Lett. , vol.11 , pp. 2019
    • Zhu, H.1    Wickenden, J.G.2    Campbell, N.E.3    Leung, J.C.T.4    Johnson, K.M.5    Sammis, G.M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.