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Volumn 53, Issue 5, 2012, Pages 564-569

A direct copper-catalyzed route to pyrrolo-fused heterocycles from boronic acids

Author keywords

Azaindoles; Boronic acids; Catalysis; Copper; Fischer rearrangement

Indexed keywords

ALDEHYDE; BORONIC ACID DERIVATIVE; COPPER; DI TERT BUTYL DIAZODICARBOXYLIC ACID; DICARBOXYLIC ACID DERIVATIVE; HETEROCYCLIC COMPOUND; INDOLE DERIVATIVE; ISOQUINOLINE DERIVATIVE; KETONE; PYRIDINE DERIVATIVE; PYRROLE; PYRROLOPYRIMIDINE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84355161848     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.11.091     Document Type: Article
Times cited : (13)

References (81)
  • 6
    • 11944265206 scopus 로고
    • Selected reviews
    • Selected reviews: P. Potier Chem. Soc. Rev. 21 1992 113 119
    • (1992) Chem. Soc. Rev. , vol.21 , pp. 113-119
    • Potier, P.1
  • 22
    • 0004061172 scopus 로고    scopus 로고
    • Indole ring formation reviews: 4th ed. Blackwell Science Publishing Oxford, UK
    • Indole ring formation reviews: J.A. Joule, and K. Mills Heterocyclic Chemistry 4th ed. 2000 Blackwell Science Publishing Oxford, UK
    • (2000) Heterocyclic Chemistry
    • Joule, J.A.1    Mills, K.2
  • 33
    • 33746864043 scopus 로고    scopus 로고
    • Fischer indole synthesis reviews
    • Fischer indole synthesis reviews: G.R. Humphrey, and J.T. Kuethe Chem. Rev. 106 2006 2875
    • (2006) Chem. Rev. , vol.106 , pp. 2875
    • Humphrey, G.R.1    Kuethe, J.T.2
  • 38
    • 77955135684 scopus 로고    scopus 로고
    • Palladium-catalyzed heteroannulation approaches to azaindoles
    • Palladium-catalyzed heteroannulation approaches to azaindoles: S.H. Spergel, D.R. Okoro, and W. Pitts J. Org. Chem. 75 2010 5316 5319
    • (2010) J. Org. Chem. , vol.75 , pp. 5316-5319
    • Spergel, S.H.1    Okoro, D.R.2    Pitts, W.3
  • 44
    • 77954560270 scopus 로고    scopus 로고
    • Donor-acceptor approaches to azaindoles
    • Donor-acceptor approaches to azaindoles: M.M. Abd Rabo Moustafa, and B.L. Pagenkopf Org. Lett. 12 2010 3168 3171
    • (2010) Org. Lett. , vol.12 , pp. 3168-3171
    • Abd Rabo Moustafa, M.M.1    Pagenkopf, B.L.2
  • 53
  • 55
    • 77955420796 scopus 로고    scopus 로고
    • Other selected recent azaindole synthesis examples
    • Other selected recent azaindole synthesis examples: A. Carpita, A. Ribecai, and P. Stabile Tetrahedron 66 2010 7169 7178
    • (2010) Tetrahedron , vol.66 , pp. 7169-7178
    • Carpita, A.1    Ribecai, A.2    Stabile, P.3
  • 63
    • 0000170983 scopus 로고
    • Organomagnesium and organolithium reagent addition to diazodicarboxylates
    • Organomagnesium and organolithium reagent addition to diazodicarboxylates: J.P. Demers, and D.H. Klaubert Tetrahedron Lett. 28 1987 4933 4934
    • (1987) Tetrahedron Lett. , vol.28 , pp. 4933-4934
    • Demers, J.P.1    Klaubert, D.H.2
  • 66
    • 26844560825 scopus 로고    scopus 로고
    • Boronic acids from pinacol boronates
    • Boronic acids from pinacol boronates: A.K.L. Yuen, and C.A. Hutton Tetrahedron Lett. 46 2005 7899 7903
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7899-7903
    • Yuen, A.K.L.1    Hutton, C.A.2
  • 72
    • 3142514770 scopus 로고
    • Typical procedure for Pd-catalyzed synthesis of aryl pinacol boronates from aryl halides
    • Typical procedure for Pd-catalyzed synthesis of aryl pinacol boronates from aryl halides: T. Ishiyama, M. Murata, and N. Miyaura J. Org. Chem. 60 1995 7508 7510
    • (1995) J. Org. Chem. , vol.60 , pp. 7508-7510
    • Ishiyama, T.1    Murata, M.2    Miyaura, N.3
  • 73
  • 80
    • 84355161367 scopus 로고    scopus 로고
    • After submission of this manuscript a similar strategy to generate indoles and some pyrrolo-fused heterocycles was described via fischer reaction of N,N-di-Boc-hydrazides generated via aryl-lithium addition to DBAD:, 10.1021/jo201866c
    • After submission of this manuscript a similar strategy to generate indoles and some pyrrolo-fused heterocycles was described via fischer reaction of N,N-di-Boc-hydrazides generated via aryl-lithium addition to DBAD: M. Inman, A. Carbone, and C.J. Moody J. Org. Chem. 2011 10.1021/jo201866c
    • (2011) J. Org. Chem.
    • Inman, M.1    Carbone, A.2    Moody, C.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.