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Volumn 9, Issue 22, 2007, Pages 4623-4626

Concise, stereoselective approach to the spirooxindole ring system of citrinadin A

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CITRINADIN A; DRUG DERIVATIVE; QUINOLIZINE DERIVATIVE; UNCLASSIFIED DRUG; VALINE;

EID: 35948974651     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702132v     Document Type: Article
Times cited : (64)

References (47)
  • 4
    • 0036796894 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Martin, S. F. Acc. Chem. Res. 2002, 35, 895.
    • (2002) Acc. Chem. Res , vol.35 , pp. 895
    • Martin, S.F.1
  • 19
    • 0038392407 scopus 로고    scopus 로고
    • For a recent review, see:, and references therein
    • For a recent review, see: Marti, C.; Carreira, E. M. Eur. J. Org. Chem. 2003, 12, 2209 and references therein.
    • (2003) Eur. J. Org. Chem , vol.12 , pp. 2209
    • Marti, C.1    Carreira, E.M.2
  • 32
    • 35949004498 scopus 로고    scopus 로고
    • Some of these results were presented at the 232nd ACS National Meeting. See: Pettersson, M.; Martin, S. F. Abstracts of Papers, 232nd ACS National Meeting, San Francisco, CA, Sep 10-14, 2006; American Chemical Society: Washington, DC, 2006; ORGN-854.
    • Some of these results were presented at the 232nd ACS National Meeting. See: Pettersson, M.; Martin, S. F. Abstracts of Papers, 232nd ACS National Meeting, San Francisco, CA, Sep 10-14, 2006; American Chemical Society: Washington, DC, 2006; ORGN-854.
  • 33
    • 35948967678 scopus 로고    scopus 로고
    • In analogy with the ome nomencalture in the biological arena, the synthome is the complete set of reactions available to the chemist for the synthesis of molecules of interest
    • In analogy with the "ome" nomencalture in the biological arena, the synthome is the complete set of reactions available to the chemist for the synthesis of molecules of interest.
  • 38
    • 4143088133 scopus 로고    scopus 로고
    • For a review on organocatalytic asymmetric epoxidations, see: c
    • For a review on organocatalytic asymmetric epoxidations, see: (c) Shi, Y. Acc. Chem. Res. 2004, 37, 488.
    • (2004) Acc. Chem. Res , vol.37 , pp. 488
    • Shi, Y.1
  • 45
    • 0037841906 scopus 로고    scopus 로고
    • Shu, L.; Wang, P.; Gan, Y.; Shi, Y. Org. Lett. 2003, 5, 293.
    • (c) Shu, L.; Wang, P.; Gan, Y.; Shi, Y. Org. Lett. 2003, 5, 293.
  • 46
    • 33745727373 scopus 로고    scopus 로고
    • N-Aryl-substituted ketone 11 prepared according to: (d) Zhao, M.-X.; Goeddel, D.; Li, K.; Shi, Y. Tetrahedron 2006, 62, 8064.
    • N-Aryl-substituted ketone 11 prepared according to: (d) Zhao, M.-X.; Goeddel, D.; Li, K.; Shi, Y. Tetrahedron 2006, 62, 8064.
  • 47
    • 35948965331 scopus 로고    scopus 로고
    • The absolute stereochemistry was established by comparing the HPLC trace of 13 derived from 12 to that of ent-13 by removal of the chiral auxiliary from 15, the stereochemistry of which was established by X-ray crystallography of 17.
    • The absolute stereochemistry was established by comparing the HPLC trace of 13 derived from 12 to that of ent-13 by removal of the chiral auxiliary from 15, the stereochemistry of which was established by X-ray crystallography of 17.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.