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Volumn 78, Issue 24, 2013, Pages 12314-12320

Recent developments in the catalytic, asymmetric construction of pyrroloindolines bearing all-carbon quaternary stereocenters

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC REACTION; NATURAL PRODUCTS; QUATERNARY STEREOCENTERS;

EID: 84890915967     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4017953     Document Type: Article
Times cited : (170)

References (69)
  • 1
    • 77957077902 scopus 로고    scopus 로고
    • Naturally Occurring Cyclotryptophans and Cyclotryptamines
    • In; Pelletier, S. W. Pergamon: Oxford, Vol.
    • Anthoni, U.; Christophersen, C.; Nielsen, P. H. Naturally Occurring Cyclotryptophans and Cyclotryptamines. In Alkaloids: Chemical & Biological Perspectives; Pelletier, S. W., Ed.; Pergamon: Oxford, 1999; Vol. 13, pp 163-236.
    • (1999) Alkaloids: Chemical & Biological Perspectives , vol.13 , pp. 163-236
    • Anthoni, U.1    Christophersen, C.2    Nielsen, P.H.3
  • 46
    • 1842586980 scopus 로고    scopus 로고
    • In the only prior enantioselective example, a 1,2-oxazine derivative was furnished in 42% ee using isovaleraldehyde as the dienophile and stoichiometric (S)-1-(2-pyrrolidinylmethyl)pyrrolidine as the chiral promoter: Wabnitz, T. C.; Saaby, S.; Jørgensen, K. A. Org. Biomol. Chem. 2004, 2, 828
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 828
    • Wabnitz, T.C.1    Saaby, S.2    Jørgensen, K.A.3
  • 54
    • 16844383145 scopus 로고    scopus 로고
    • For related prior research involving the non-asymmetric triethylborane-catalyzed allylation of 3-methylindole, see: Kimura, M.; Futamata, M.; Mukai, R.; Tamaru, Y. J. Am. Chem. Soc. 2005, 127, 4592
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4592
    • Kimura, M.1    Futamata, M.2    Mukai, R.3    Tamaru, Y.4
  • 55
    • 84873970915 scopus 로고    scopus 로고
    • For a recent report of Pd-catalyzed AAA reactions of indoles using allyl carbonates, see: Liu, Y.; Du, H. Org. Lett. 2013, 15, 740
    • (2013) Org. Lett. , vol.15 , pp. 740
    • Liu, Y.1    Du, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.