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Volumn 63, Issue 3, 1998, Pages 543-550

Synthesis and characterization of a highly potent and selective isotopically labeled retinoic acid receptor ligand, ALRT1550

Author keywords

[No Author keywords available]

Indexed keywords

7 (3,5 DI TERT BUTYLPHENYL) 3 METHYL 2,4,6 OCTATRIENOIC ACID; ALITRETINOIN; RETINOIC ACID; RETINOIC ACID DERIVATIVE; RETINOIC ACID RECEPTOR; RETINOID; RETINOID X RECEPTOR; UNCLASSIFIED DRUG;

EID: 0032489022     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971409i     Document Type: Article
Times cited : (17)

References (32)
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  • 25
    • 6844254241 scopus 로고
    • 3SnH conditions (see Parnes, H.; Pease, J. J. Org. Chem. 1979, 44, 151-152); reduction of the tosylate derived from 26 (TsCl, Py neat, 84%) using lithium triethylborohydride according to Binkley, R. W. J. Org. Chem. 1985, 50, 5646-5649. For LAH reduction of neopentylic tosylates, see: Collins, D. J.; Jacobs, H. A. Aust. J. Chem. 1986, 39, 2095-2110.
    • (1985) J. Org. Chem. , vol.107 , pp. 1448
    • Curran, D.P.1    Rakiewicz, D.M.2
  • 26
    • 0010831188 scopus 로고
    • 3SnH conditions (see Parnes, H.; Pease, J. J. Org. Chem. 1979, 44, 151-152); reduction of the tosylate derived from 26 (TsCl, Py neat, 84%) using lithium triethylborohydride according to Binkley, R. W. J. Org. Chem. 1985, 50, 5646-5649. For LAH reduction of neopentylic tosylates, see: Collins, D. J.; Jacobs, H. A. Aust. J. Chem. 1986, 39, 2095-2110.
    • (1979) J. Org. Chem. , vol.44 , pp. 151-152
    • Parnes, H.1    Pease, J.2
  • 27
    • 0007052797 scopus 로고
    • 3SnH conditions (see Parnes, H.; Pease, J. J. Org. Chem. 1979, 44, 151-152); reduction of the tosylate derived from 26 (TsCl, Py neat, 84%) using lithium triethylborohydride according to Binkley, R. W. J. Org. Chem. 1985, 50, 5646-5649. For LAH reduction of neopentylic tosylates, see: Collins, D. J.; Jacobs, H. A. Aust. J. Chem. 1986, 39, 2095-2110.
    • (1985) J. Org. Chem. , vol.50 , pp. 5646-5649
    • Binkley, R.W.1
  • 28
    • 3342879774 scopus 로고
    • 3SnH conditions (see Parnes, H.; Pease, J. J. Org. Chem. 1979, 44, 151-152); reduction of the tosylate derived from 26 (TsCl, Py neat, 84%) using lithium triethylborohydride according to Binkley, R. W. J. Org. Chem. 1985, 50, 5646-5649. For LAH reduction of neopentylic tosylates, see: Collins, D. J.; Jacobs, H. A. Aust. J. Chem. 1986, 39, 2095-2110.
    • (1986) Aust. J. Chem. , vol.39 , pp. 2095-2110
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  • 29
    • 0027402432 scopus 로고
    • For Zn/AcOH reduction of neopentylic iodides, see: Ito, M.; Kibayashi, C. Synthesis 1993, 137-140.
    • (1993) Synthesis , pp. 137-140
    • Ito, M.1    Kibayashi, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.