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Volumn 126, Issue 7, 2004, Pages 1954-1955

Construction of Arene-Fused-Piperidine Motifs by Asymmetric Addition of 2-Trityloxymethylaryllithiums to Nitroalkenes: The Asymmetric Synthesis of a Dopamine D1 Full Agonist, A-86929

Author keywords

[No Author keywords available]

Indexed keywords

2 TRITYLOXYMETHYLLITHIUM; 4,5,5A,6,7,11B HEXAHYDRO 9,10 DIHYDROXY 2 PROPYL 3 THIA 5 AZACYCLOPENT 1 ENA[C]PHENANTHRENE; ALKENE; LITHIUM; NITROALKENE; PIPERIDINE; POLYCYCLIC AROMATIC HYDROCARBON; UNCLASSIFIED DRUG;

EID: 1242342197     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja031760n     Document Type: Article
Times cited : (61)

References (37)
  • 1
    • 77957033352 scopus 로고
    • Brossi, A., Ed.; Academic Press: New York
    • Reviews: (a) Martin, S. F. In The Alkaloids; Brossi, A., Ed.; Academic Press: New York, 1987; Vol. 30, pp 251-376.
    • (1987) The Alkaloids , vol.30 , pp. 251-376
    • Martin, S.F.1
  • 4
    • 77956708370 scopus 로고    scopus 로고
    • Cordell, G. A., Ed.: Academic Press: San Diego
    • (d) Hoshino, O. In The Alkaloids; Cordell, G. A., Ed.: Academic Press: San Diego, 1998; Vol. 51, pp 323-424.
    • (1998) The Alkaloids , vol.51 , pp. 323-424
    • Hoshino, O.1
  • 8
    • 1942471590 scopus 로고    scopus 로고
    • Galantamine: (d) WHO Drug Inf. 1998, 12, 205.
    • (1998) WHO Drug Inf. , vol.12 , pp. 205
  • 23
    • 0000679263 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Chapter 31
    • (b) Tomioka, K.; Nagaoka, Y. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. 111, Chapter 31.
    • (1999) Comprehensive Asymmetric Catalysis , vol.111
    • Tomioka, K.1    Nagaoka, Y.2
  • 24
    • 1242281489 scopus 로고    scopus 로고
    • Otera, J., Ed.; Wiley-VCH: Weinheim; Chapter 12
    • (c) Tomioka, K. In Modern Carbonyl Chemistry; Otera, J., Ed.; Wiley-VCH: Weinheim, 2000; Chapter 12.
    • (2000) Modern Carbonyl Chemistry
    • Tomioka, K.1
  • 34
    • 1242348801 scopus 로고    scopus 로고
    • note
    • 4Cl.
  • 35
    • 1242348800 scopus 로고    scopus 로고
    • note
    • The shown absolute configurations of 4a-c, 14c, and 15 were determined by conversion to known compounds. See Supporting lnformation.
  • 36
    • 1242303777 scopus 로고    scopus 로고
    • note
    • The reactions of other aryllithiums having a bulky substituent at the ortho position also gave products in good selectivities. See Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.