메뉴 건너뛰기




Volumn , Issue 2, 2006, Pages 309-314

Deacylation of esters, thioesters and amides by a naphthalene-catalysed lithiation

Author keywords

Amides; Deacylation; Esters; Lithium; Thioesters

Indexed keywords

CARBOHYDRATES; CATALYSIS; LITHIUM; NAPHTHALENE; NITROGEN COMPOUNDS;

EID: 31544451300     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-918501     Document Type: Article
Times cited : (20)

References (58)
  • 1
    • 0003417469 scopus 로고
    • Trost, B. M.; Fleming, I.; Winterfeldt, E., Eds.; Pergamon Press: Oxford, Chap. 3.1
    • (a) Kunz, H.; Waldmann, H. In Comprehensive Organic Synthesis, Vol. 6; Trost, B. M.; Fleming, I.; Winterfeldt, E., Eds.; Pergamon Press: Oxford, 1991, Chap. 3.1.
    • (1991) Comprehensive Organic Synthesis , vol.6
    • Kunz, H.1    Waldmann, H.2
  • 10
  • 11
    • 0030496093 scopus 로고    scopus 로고
    • For reviews, see: (a) Yus, M. Chem. Soc. Rev. 1996, 25, 155.
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 155
    • Yus, M.1
  • 13
    • 0034904455 scopus 로고    scopus 로고
    • (c) Yus, M. Synlett 2001, 1197.
    • (2001) Synlett , pp. 1197
    • Yus, M.1
  • 16
    • 31544447985 scopus 로고    scopus 로고
    • Rappoport, Z.; Mareck, I., Eds.; J. Wiley & Sons: Chichester, Chap. 11
    • (f) Yus, M. In The Chemistry of Organolithium Compounds; Rappoport, Z.; Mareck, I., Eds.; J. Wiley & Sons: Chichester, 2004, Chap. 11.
    • (2004) The Chemistry of Organolithium Compounds
    • Yus, M.1
  • 24
    • 0001143848 scopus 로고    scopus 로고
    • This methodology has been extensively used in our laboratories, see: (a) Generation of organolithium compounds from non-halogenated materials: Guijarro, D.; Yus, M. Recent Res. Dev. Org. Chem. 1998, 2, 713. Preparation of very sensitive functionalised organolithium compounds:
    • (1998) Recent Res. Dev. Org. Chem. , vol.2 , pp. 713
    • Guijarro, D.1    Yus, M.2
  • 30
    • 23944484430 scopus 로고    scopus 로고
    • (g) See also the special issue of Tetrahedron Symposium in Print devoted to 'Functionalised Organolithium Compounds', Nájera, C.; Yus, M., Guest Eds.; Tetrahedron 2005, 61, 3125. Reductive ring-opening of heterocycles:
    • (2005) Tetrahedron , vol.61 , pp. 3125
    • Nájera, C.1    Yus, M.2
  • 33
    • 0141988919 scopus 로고    scopus 로고
    • (j) Yus, M. Pure Appl. Chem. 2003, 75, 1453. Generation of polylithium synthons:
    • (2003) Pure Appl. Chem. , vol.75 , pp. 1453
    • Yus, M.1
  • 43
    • 0033520272 scopus 로고    scopus 로고
    • and references cited therein
    • For a related paper from our group on the generation of allylic and benzylic organolithium intermediates from the corresponding carbonates, carbamates and ureas, see: Alonso, E.; Guijarro, D.; Martinez, P.; Ramon, D. J.; Yus, M. Tetrahedron 1999, 55, 11027; and references cited therein.
    • (1999) Tetrahedron , vol.55 , pp. 11027
    • Alonso, E.1    Guijarro, D.2    Martinez, P.3    Ramon, D.J.4    Yus, M.5
  • 44
    • 0012145612 scopus 로고
    • A similar transformation of aromatic esters into 1,2-diarylethanes by a DTBB-catalysed lithiation under sonication has been reported: Karaman, R.; Fry, J. L. Tetrahedron Lett. 1989, 30, 4931.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 4931
    • Karaman, R.1    Fry, J.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.