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Volumn 12, Issue 14, 2004, Pages 3931-3942

Preparation and biological activity of 13-substituted retinoic acids

Author keywords

Coupling reaction; RAR; Retinoic acid analogs; RXR

Indexed keywords

3 BUTYL 7 METHYL 9 (2,6,6 TRIMETHYL 1 CYCLOHEXEN 1 YL) 2,4,6,8 NONATETRAENOIC ACID; 3 ETHYL 7 METHYL 9 (2,6,6 TRIMETHYL 1 CYCLOHEXEN 1 YL) 2,4,6,8 NONATETRAENOIC ACID; 7 METHYL 3 (2 PHENYL)ETHYL 9 (2,6,6 TRIMETHYL 1 CYCLOHEXEN 1 YL) 2,4,6,8 NONATETRAENOIC ACID; 7 METHYL 3 PROPYL 9 (2,6,6 TRIMETHYL 1 CYCLOHEXEN 1 YL) 2,4,6,8 NONATETRAENOIC ACID; RETINOIC ACID; RETINOIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 2942729585     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2004.04.047     Document Type: Article
Times cited : (21)

References (39)
  • 19
    • 0028861864 scopus 로고
    • Several similar cross-coupling reactions for the stereoselective synthesis of retinoids have already been reported. For all-E-retinoids:
    • Several similar cross-coupling reactions for the stereoselective synthesis of retinoids have already been reported. For all-E-retinoids: Torrado A., Iglesias B., López S., de Lera A.R. Tetrahedron. 51:1995;2435
    • (1995) Tetrahedron , vol.51 , pp. 2435
    • Torrado, A.1    Iglesias, B.2    López, S.3    De Lera, A.R.4
  • 29
    • 2942756449 scopus 로고    scopus 로고
    • note
    • We found that this catalyst system is more effective than tetrakistriphenylphosphine palladium(0) for the coupling reaction of vinyl stannane with vinyl triflate (see Ref. [6a])


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.