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Volumn 2007, Issue 7, 2007, Pages 41-50

Reductive removal of the Boc protecting group via a DTBB-catalysed lithiation reaction

Author keywords

Alcohols; Amines; Boc; Deprotection; DTBB; Lithium; tert butoxycarbonyl; Thiols

Indexed keywords


EID: 33846263724     PISSN: 1551-7012     EISSN: 14246376     Source Type: Journal    
DOI: 10.3998/ark.5550190.0008.706     Document Type: Article
Times cited : (5)

References (55)
  • 2
    • 0001295905 scopus 로고
    • For a review, see
    • (b) For a review, see: Carpino, L. A. Acc. Chem. Res. 1973, 6, 191.
    • (1973) Acc. Chem. Res , vol.6 , pp. 191
    • Carpino, L.A.1
  • 3
    • 0003417469 scopus 로고
    • Trost, B. M, Fleming, I, Winterfeldt, E, Eds, Pergamon Press: Oxford, Chapter 3.1
    • Kunz, H.; Waldmann, H. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Winterfeldt, E., Eds.; Pergamon Press: Oxford, 1991; Vol. 6; Chapter 3.1.
    • (1991) Comprehensive Organic Synthesis , vol.6
    • Kunz, H.1    Waldmann, H.2
  • 13
    • 0030496093 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Yus, M. Chem. Soc. Rev. 1996, 25, 155.
    • (1996) Chem. Soc. Rev , vol.25 , pp. 155
    • Yus, M.1
  • 15
    • 0034904455 scopus 로고    scopus 로고
    • (c) Yus, M. Synlett 2001, 1197.
    • (2001) Synlett , pp. 1197
    • Yus, M.1
  • 16
    • 0002156550 scopus 로고    scopus 로고
    • (d) Yus, M.; Ramón, D. J. Latv. J. Chem. 2002, 79.
    • (2002) J. Chem , pp. 79
    • Yus, M.1
  • 18
    • 85069138885 scopus 로고    scopus 로고
    • Rappoport, Z, Mareck, I, Eds, J. Wiley & Sons: Chichester, Chapter 11
    • (f) Yus, M. In The Chemistry of Organolithium Compounds; Rappoport, Z.; Mareck, I., Eds.; J. Wiley & Sons: Chichester, 2004; Chapter 11.
    • (2004) The Chemistry of Organolithium Compounds
    • Yus, M.1
  • 22
    • 0032510282 scopus 로고    scopus 로고
    • For a polymer version of this reaction, see: a
    • For a polymer version of this reaction, see: (a) Gómez, C.; Ruiz, S.; Yus, M. Tetrahedron Lett. 1998, 39, 1397.
    • (1998) Tetrahedron Lett , vol.39 , pp. 1397
    • Gómez, C.1    Ruiz, S.2    Yus, M.3
  • 26
    • 85069129113 scopus 로고    scopus 로고
    • This methodology has been extensively used in our laboratories for the following applications: generation of organolithium compounds from non-halogenated materials,14a preparation of very sensitive functionalised organolithium compounds,14b-g reductive ring-opening of heterocycles,14h-j generation of polylithium synthons 14k,l and for the activation of other metals,14m especially nickel.14n,o For reviews from our group, see: (a) Guijarro, D, Yus, M. Recent Res. Dev. Org. Chem. 1998, 2, 713
    • 14n,o For reviews from our group, see: (a) Guijarro, D.; Yus, M. Recent Res. Dev. Org. Chem. 1998, 2, 713.
  • 32
    • 85069141513 scopus 로고    scopus 로고
    • See also the especial issue of Tetrahedron Symposium in Print devoted to Functionalised Organolithium Compounds Nájera, C.; Yus, M., Guest Eds., Tetrahedron 2005, 61, 3125.
    • (g) See also the especial issue of Tetrahedron Symposium in Print devoted to "Functionalised Organolithium Compounds" Nájera, C.; Yus, M., Guest Eds., Tetrahedron 2005, 61, 3125.
  • 46
    • 85086954233 scopus 로고    scopus 로고
    • th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-9), communication no A009.
    • th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-9), communication no A009.
  • 50
    • 85069143004 scopus 로고    scopus 로고
    • Chem. Abstr. 1986, 104, 225267.
    • Chem. Abstr. 1986, 104, 225267.
  • 52
    • 85069135065 scopus 로고
    • Jpn. Kokai Tokkyo Koho, JP 06128198;, 80875
    • Iwasaki, F. Jpn. Kokai Tokkyo Koho 1994, JP 06128198; Chem. Abstr. 1994, 122, 80875.
    • (1994) Chem. Abstr , vol.122
    • Iwasaki, F.1
  • 55


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.