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Volumn , Issue 17, 2008, Pages 2805-2818

N-heterocyclic carbene catalysed oxygen-to-carbon carboxyl transfer of indolyl and benzofuranyl carbonates

Author keywords

Carboxyl transfer; Catalysis; N heterocyclic carbene

Indexed keywords

NONMETALS; OXYGEN;

EID: 51949090002     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1077890     Document Type: Article
Times cited : (41)

References (78)
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    • 2nd ed, Ojima, I, Ed, Wiley-VCH: New York
    • (a) O'Donnell, M. J. In Catalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; Wiley-VCH: New York, 2000, 727-755.
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    • For asymmetric versions of this reaction, see: a
    • For asymmetric versions of this reaction, see: (a) Ruble, J. C.; Fu, G. C. J. Am. Chem. Soc. 1998, 120, 11532.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 11532
    • Ruble, J.C.1    Fu, G.C.2
  • 64
    • 0042819678 scopus 로고    scopus 로고
    • For the application of this methodology to the preparation of oxindole and benzofuran derivatives, see
    • (f) For the application of this methodology to the preparation of oxindole and benzofuran derivatives, see: Hills, I. D.; Fu, G. C. Angew. Chem. Int. Ed. 2003, 42, 3921.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 3921
    • Hills, I.D.1    Fu, G.C.2
  • 65
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    • For the seminal work of Black upon the rearrangement of benzofuranyl carbonates with DMAP, see: a
    • For the seminal work of Black upon the rearrangement of benzofuranyl carbonates with DMAP, see: (a) Black, T. H.; Arrivo, S. M.; Schumm, J. S.; Knobeloch, J. M. J. Chem. Soc., Chem. Commun. 1986, 1524.
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    • Wiemer et al. have demonstrated extensively the base-catalysed rearrangement of vinyl phosphates to the corresponding β-keto phosphonates; a process driven under thermodynamic control by the formation of a stabilised anion. For an example, see
    • Wiemer et al. have demonstrated extensively the base-catalysed rearrangement of vinyl phosphates to the corresponding β-keto phosphonates; a process driven under thermodynamic control by the formation of a stabilised anion. For an example, see: Calogeropoulou, T.; Hammond, G. B.; Wiemer, D. F. J. Org. Chem. 1987, 52, 4185.
    • (1987) J. Org. Chem , vol.52 , pp. 4185
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    • U.S. Patent 2759935, 9613
    • Speeter, M. E. U.S. Patent 2759935, 1956; Chem. Abstr. 1956, 51, 9613.
    • (1956) Chem. Abstr , vol.51
    • Speeter, M.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.