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Volumn 50, Issue 50, 2009, Pages 6977-6980

Acyclic ketene aminal phosphates derived from N,N-diprotected acetamides: stability and cross-couplings

Author keywords

Catalysis; Diene; Enyne; Stille reaction; Suzuki reaction

Indexed keywords

ACETAMIDE DERIVATIVE; ALKADIENE; ALPHA PHOSPHORYLOXY ENECARBAMATE; CARBAMIC ACID DERIVATIVE; ENEDIYNE; KETENE AMINAL PHOSPHATE; KETENE DERIVATIVE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 70350761890     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.09.159     Document Type: Article
Times cited : (15)

References (39)
  • 1
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    • Tsuji J. (Ed), Springer, Berlin/Heidelberg
    • In: Tsuji J. (Ed). Palladium in Organic Synthesis (2005), Springer, Berlin/Heidelberg
    • (2005) Palladium in Organic Synthesis
  • 20
    • 0035817206 scopus 로고    scopus 로고
    • The following works dealt with the stability problem in cyclic ketene aminal phosphates and triflates. Our experience has shown that the acyclic counterparts may be as labile as the ones derived from five-membered lactams (Ref. 8a):
    • The following works dealt with the stability problem in cyclic ketene aminal phosphates and triflates. Our experience has shown that the acyclic counterparts may be as labile as the ones derived from five-membered lactams (Ref. 8a):. Lepifre F., Clavier S., Bouyssou P., and Coudert G. Tetrahedron 57 (2001) 6969
    • (2001) Tetrahedron , vol.57 , pp. 6969
    • Lepifre, F.1    Clavier, S.2    Bouyssou, P.3    Coudert, G.4
  • 21
    • 70350755145 scopus 로고    scopus 로고
    • See Ref. 3c
    • See Ref. 3c.
  • 32
    • 51049124099 scopus 로고    scopus 로고
    • Stannane 17b was prepared by hydrostannylation of 3-butyn-1-ol under the conditions advanced by Chong's group, followed by O-methylation:
    • Stannane 17b was prepared by hydrostannylation of 3-butyn-1-ol under the conditions advanced by Chong's group, followed by O-methylation:. Darwish A., Lang A., Kim T., and Chong J.M. Org. Lett. 10 (2008) 861
    • (2008) Org. Lett. , vol.10 , pp. 861
    • Darwish, A.1    Lang, A.2    Kim, T.3    Chong, J.M.4
  • 35
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    • note
    • +).
  • 36
    • 70350781897 scopus 로고    scopus 로고
    • note
    • -1.
  • 37
    • 0030593682 scopus 로고    scopus 로고
    • Enynes and dienes displaying similar functional features, for the most part, have been incidentally generated:
    • Enynes and dienes displaying similar functional features, for the most part, have been incidentally generated:. Meffre P., Gauzy L., Branquet E., Durand P., and Le Goffic F. Tetrahedron 52 (1996) 11215
    • (1996) Tetrahedron , vol.52 , pp. 11215
    • Meffre, P.1    Gauzy, L.2    Branquet, E.3    Durand, P.4    Le Goffic, F.5
  • 39
    • 0034647926 scopus 로고    scopus 로고
    • For a designed methodology towards similar enyne via a double elimination:
    • For a designed methodology towards similar enyne via a double elimination:. Saito S., Uchiyama N., Gevorgyan V., and Yamamoto Y. J. Org. Chem. 65 (2001) 4338
    • (2001) J. Org. Chem. , vol.65 , pp. 4338
    • Saito, S.1    Uchiyama, N.2    Gevorgyan, V.3    Yamamoto, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.