메뉴 건너뛰기




Volumn 50, Issue 48, 2009, Pages 6665-6667

Triflic anhydride-mediated tandem formylation/cyclization of cyanoacetanilides: a concise synthesis of glycocitlone alkaloids

Author keywords

[No Author keywords available]

Indexed keywords

ACETANILIDE DERIVATIVE; ALKALOID DERIVATIVE; CYANOACETANILIDE DERIVATIVE; GLYCOCITLONE A; GLYCOCITLONE C; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

EID: 70349974245     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.09.073     Document Type: Article
Times cited : (18)

References (52)
  • 2
    • 38849111840 scopus 로고    scopus 로고
    • For recent reviews, see: and earlier annual reviews in this journal by the same author
    • For recent reviews, see:. Michael J.P. Nat. Prod. Rep. 25 (2008) 166-187 and earlier annual reviews in this journal by the same author
    • (2008) Nat. Prod. Rep. , vol.25 , pp. 166-187
    • Michael, J.P.1
  • 10
    • 33644839988 scopus 로고    scopus 로고
    • For diversity-oriented synthesis, see:
    • For diversity-oriented synthesis, see:. Tan D.S. Nat. Chem. Biol. 1 (2005) 74-84
    • (2005) Nat. Chem. Biol. , vol.1 , pp. 74-84
    • Tan, D.S.1
  • 18
    • 31544434530 scopus 로고    scopus 로고
    • For recent reviews, see:
    • For recent reviews, see:. Dömling A. Chem. Rev. 106 (2006) 17-89
    • (2006) Chem. Rev. , vol.106 , pp. 17-89
    • Dömling, A.1
  • 25
    • 0040335536 scopus 로고
    • For the stepwise preparation of 3-formyl-4-hydroxyquinolin-2(1H)-ones, see:
    • For the stepwise preparation of 3-formyl-4-hydroxyquinolin-2(1H)-ones, see:. Tomita K. J. Pharm. Soc. Jpn. 71 (1951) 1100-1112
    • (1951) J. Pharm. Soc. Jpn. , vol.71 , pp. 1100-1112
    • Tomita, K.1
  • 27
    • 64349096396 scopus 로고    scopus 로고
    • All cyanoacetanilides 6a-j were easily prepared, purified, and obtained as solids; see the Supplementary data. Also see:
    • All cyanoacetanilides 6a-j were easily prepared, purified, and obtained as solids; see the Supplementary data. Also see:. Kobayashi Y., and Harayama T. Org. Lett. 11 (2009) 1603-1606
    • (2009) Org. Lett. , vol.11 , pp. 1603-1606
    • Kobayashi, Y.1    Harayama, T.2
  • 28
    • 70349901715 scopus 로고    scopus 로고
    • note
    • 7 (13 equiv).
  • 29
    • 0001586671 scopus 로고
    • For reviews of Friedel-Crafts and related reactions, see:. Trost B.M., and Fleming I. (Eds), Pergamon, Oxford Chapter 1.8
    • For reviews of Friedel-Crafts and related reactions, see:. Olah G.A., Krishnamurti R., and Prakash G.S.S. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 3 (1991), Pergamon, Oxford Chapter 1.8
    • (1991) Comprehensive Organic Synthesis , vol.3
    • Olah, G.A.1    Krishnamurti, R.2    Prakash, G.S.S.3
  • 34
    • 0002556521 scopus 로고    scopus 로고
    • The Vilsmeier Reaction of Fully Conjugated Carbocycles and Heterocycles
    • For reviews, see:. Paquette L.A. (Ed), John Wiley, New York
    • For reviews, see:. Jones G., and Stanforth S.P. The Vilsmeier Reaction of Fully Conjugated Carbocycles and Heterocycles. In: Paquette L.A. (Ed). Organic Reactions Vol. 49 (1997), John Wiley, New York 1-330
    • (1997) Organic Reactions , vol.49 , pp. 1-330
    • Jones, G.1    Stanforth, S.P.2
  • 36
    • 0000600789 scopus 로고
    • Iminium Salts in Organic Chemistry
    • Taylor E.C. (Ed), John Wiley & Sons, New York
    • Jutz C. Iminium Salts in Organic Chemistry. In: Taylor E.C. (Ed). Advances in Organic Chemistry Vol. 9, Part I (1976), John Wiley & Sons, New York 225-342
    • (1976) Advances in Organic Chemistry , vol.9 PART I , pp. 225-342
    • Jutz, C.1
  • 38
    • 68349097558 scopus 로고    scopus 로고
    • For examples of the synthesis of quinolines under Vilsmeier conditions, see:
    • For examples of the synthesis of quinolines under Vilsmeier conditions, see:. Wang Y., Xin X., Liang Y., Lin Y., Zhang R., and Dong D. Eur. J. Org. Chem. (2009) 4165-4169
    • (2009) Eur. J. Org. Chem. , pp. 4165-4169
    • Wang, Y.1    Xin, X.2    Liang, Y.3    Lin, Y.4    Zhang, R.5    Dong, D.6
  • 52
    • 1542345321 scopus 로고    scopus 로고
    • For the Pd-catalyzed addition of C-H to nitrile, see:
    • For the Pd-catalyzed addition of C-H to nitrile, see:. Zhou C., and Larock R.C. J. Am. Chem. Soc. 126 (2004) 2302-2303
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2302-2303
    • Zhou, C.1    Larock, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.