메뉴 건너뛰기




Volumn 4, Issue 8, 2015, Pages 694-708

Nucleophilic Nitrenoids Through π-Acid Catalysis: Providing a Common Basis for Rapid Access into Diverse Nitrogen Heterocycles

Author keywords

Cyclizations; Gold carbenes; Heterocycles; Nitrenoids; acid catalysis

Indexed keywords


EID: 84938703483     PISSN: 21935807     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajoc.201500170     Document Type: Review
Times cited : (106)

References (101)
  • 1
    • 84891285203 scopus 로고    scopus 로고
    • Amino-Based Building Blocks for the Construction of Biomolecules: in (Ed.: A. Ricci), Wiley-VCH, Weinheim, 592;
    • "Amino-Based Building Blocks for the Construction of Biomolecules": A. Mann in Amino Group Chemistry: From Synthesis to the Life Sciences (Ed.: A. Ricci), Wiley-VCH, Weinheim, 2007, pp.207-256-592;.
    • (2007) Amino Group Chemistry: From Synthesis to the Life Sciences , pp. 207-256
    • Mann, A.1
  • 4
    • 28744441905 scopus 로고    scopus 로고
    • Ed.: S.A. Lawrence), Cambridge University Press, Cambridge
    • Amines: Synthesis Properties and Applications (Ed.: S.A. Lawrence), Cambridge University Press, Cambridge, 2004;.
    • (2004) Amines: Synthesis Properties and Applications
  • 5
    • 84956794765 scopus 로고    scopus 로고
    • Ed.: A. Ricci), Wiley-VCH, Weinheim
    • Modern Amination Methods (Ed.: A. Ricci), Wiley-VCH, Weinheim, 2007.
    • (2007) Modern Amination Methods
  • 6
  • 18
    • 4544256467 scopus 로고    scopus 로고
    • Synthetic Carbene and Nitrene Chemistry
    • (Eds.: R.A. Moss, M.S. Platz, M. Jones,Jr.), Wiley Interscience, New York
    • "Synthetic Carbene and Nitrene Chemistry": M. P. Doyle in Reactive Intermediate Chemistry (Eds.: R.A. Moss, M.S. Platz, M. Jones, Jr.), Wiley Interscience, New York, 2004, pp.561-592.
    • (2004) Reactive Intermediate Chemistry , pp. 561-592
    • Doyle, M.P.1
  • 24
    • 84938717368 scopus 로고    scopus 로고
    • The issue of at what stage the nucleofuge is eliminated and how it can affect reactivity is also relevant in the closely related use of nucleophilic oxidants to access α-oxo gold carbene reactivity from triple bonds. For recent representative overviews of this field or examples discussing that aspect:
    • The issue of at what stage the nucleofuge is eliminated and how it can affect reactivity is also relevant in the closely related use of nucleophilic oxidants to access α-oxo gold carbene reactivity from triple bonds. For recent representative overviews of this field or examples discussing that aspect:.
  • 31
    • 84899862031 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 4907-4911
    • G. Seidel, A. Fürstner, Angew. Chem. Int. Ed. 2014, 53, 4807-4811; Angew. Chem. 2014, 126, 4907-4911;.
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 4807-4811
    • Seidel, G.1    Fürstner, A.2
  • 32
    • 77954837014 scopus 로고    scopus 로고
    • Angew. Chem. 2010, 122, 5360-5369
    • A. S. K. Hashmi, Angew. Chem. Int. Ed. 2010, 49, 5232-5241; Angew. Chem. 2010, 122, 5360-5369;.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 5232-5241
    • Hashmi, A.S.K.1
  • 36
  • 52
    • 79960909487 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 7492-7496;
    • A. Wetzel, F. Gagosz, Angew. Chem. Int. Ed. 2011, 50, 7354-7358; Angew. Chem. 2011, 123, 7492-7496;.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7354-7358
    • Wetzel, A.1    Gagosz, F.2
  • 62
    • 79957991334 scopus 로고    scopus 로고
    • and references therein.
    • W. He, C. Li, L. Zhang, J. Am. Chem. Soc. 2011, 133, 8482-8485 and references therein.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 8482-8485
    • He, W.1    Li, C.2    Zhang, L.3
  • 70
    • 79953205629 scopus 로고    scopus 로고
    • alkyne
    • C. Li, L. Zhang, Org. Lett. 2011, 13, 1738-1741; alkyne.
    • (2011) Org. Lett. , vol.13 , pp. 1738-1741
    • Li, C.1    Zhang, L.2
  • 78
    • 84906101626 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 9218-9222
    • S. N. Karad, R.-S. Liu, Angew. Chem. Int. Ed. 2014, 53, 9072-9076; Angew. Chem. 2014, 126, 9218-9222;.
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 9072-9076
    • Karad, S.N.1    Liu, R.-S.2
  • 95
    • 84860741341 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 4759-4762
    • S. Kramer, T. Skrydstrup, Angew. Chem. Int. Ed. 2012, 51, 4681-4684; Angew. Chem. 2012, 124, 4759-4762;.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 4681-4684
    • Kramer, S.1    Skrydstrup, T.2
  • 98
    • 84896394097 scopus 로고    scopus 로고
    • For an alternative non-nintrenoid gold-catalyzed synthesis of imidazo[1,2-a]pyridines
    • For an alternative non-nintrenoid gold-catalyzed synthesis of imidazo[1, 2-a]pyridines: E. P. A. Talbot, M. Richardson, J. M. McKenna, F. D. Toste, Adv. Synth. Catal. 2014, 356, 687-691.
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 687-691
    • Talbot, E.P.A.1    Richardson, M.2    McKenna, J.M.3    Toste, F.D.4
  • 101
    • 84922626831 scopus 로고    scopus 로고
    • Contrasting with the non-nitrenoid intermolecular reactions of 2H-azirines with terminal alkynes under copper catalysis
    • Contrasting with the non-nitrenoid intermolecular reactions of 2H-azirines with terminal alkynes under copper catalysis: T. Li, C. Wang, D. Wang, F. Wu, X. Li, B. Wan, Org. Lett. 2014, 16, 4806-4809.
    • (2014) Org. Lett. , vol.16 , pp. 4806-4809
    • Li, T.1    Wang, C.2    Wang, D.3    Wu, F.4    Li, X.5    Wan, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.