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Volumn 17, Issue 4, 2006, Pages 590-597

Studies on Cu-catalyzed asymmetric alkynylation of tetrahydroisoquinoline derivatives

Author keywords

[No Author keywords available]

Indexed keywords

1 (4 BROMOPHENYLETHYNYL)2 PHENYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 1 (4 METHOXYPHENYLETHYNYL)2 PHENYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 1 OCT 1 YNYL 2 PHENYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 1,2,3,4 TETRAHYDRO 2 (2 METHOXYPHENYL)ISOQUINOLINE; 1,2,3,4 TETRAHYDRO 2 (4 METHOXYPHENYL)ISOQUINOLINE; 1,2,3,4 TETRAHYDRO 2 PHENYLISOQUINOLINE; 2 (2 BROMOPHENYL) 2 (2 METHOXYPHENYL) 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 (2 METHOXYPHENYL) 1 (4 METHOXYPHENYL) 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 (2 METHOXYPHENYL) 1 PYRIDIN 2 YLETHYNYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 (2 METHOXYPHENYL)1 PHENYLETHYNYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 (4 METHOXYPHENYL)1 OCT 1 YNYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 (4 METHOXYPHENYL)1 PHENYLETHYNYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 [2 (2 METHOXYETHOXY)PHENYL] 1 [2 (4 BROMOPHENYL)ETHYNYL] 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 [2 (2 METHOXYETHOXY)PHENYL] 1,2,3,4 TETRAHYDRO 1 (2 PHENYLETHYNYL) ISOQUINOLINE; 2 [2 (2 METHOXYETHOXY)PHENYL] 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 PHENYL 1 PHENYLETHYNYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 2 PHENYL 1 TRIMETHYLSILANYLETHYNYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 3,4 DIHYDRO 2 PHENYL ISOQUINOLINIUM BROMIDE; 3,4 DIHYDRO 2 PHENYL ISOQUINOLINIUM TRIFLATE; COPPER; TETRAHYDROISOQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33645857392     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.02.007     Document Type: Article
Times cited : (148)

References (46)
  • 1
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    • For representative recent reviews, see:
    • For representative recent reviews, see:. Bentley K.W. Nat. Prod. Rep. 22 (2005) 249
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    • Bentley, K.W.1
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    • Ref. 1a.
  • 8
    • 3242666141 scopus 로고    scopus 로고
    • For representative multi-step syntheses of alkynyl tetrahydroisoquinoline derivatives:
    • For representative multi-step syntheses of alkynyl tetrahydroisoquinoline derivatives:. Ukhin L.Y., Golding I.R., and Kartsev V.G. Chem. Nat. Compd. 40 (2004) 156
    • (2004) Chem. Nat. Compd. , vol.40 , pp. 156
    • Ukhin, L.Y.1    Golding, I.R.2    Kartsev, V.G.3
  • 11
    • 2942528733 scopus 로고    scopus 로고
    • For asymmetric addition of an aryl C-H bond, see: and references cited therein
    • For asymmetric addition of an aryl C-H bond, see:. Thalji R.K., Ellman J.A., and Bergman R.G. J. Am. Chem. Soc. 126 (2004) 7192 and references cited therein
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 7192
    • Thalji, R.K.1    Ellman, J.A.2    Bergman, R.G.3
  • 12
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    • For asymmteric addition of alkynyl C-H bonds, see:
    • For asymmteric addition of alkynyl C-H bonds, see:. Wei C., Li Z., and Li C.-J. Synlett (2004) 1472
    • (2004) Synlett , pp. 1472
    • Wei, C.1    Li, Z.2    Li, C.-J.3
  • 41
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    • Recently, enantioselective addition of terminal alkynes to isoquinoline iminium was reported:
    • Recently, enantioselective addition of terminal alkynes to isoquinoline iminium was reported:. Taylor A.M., and Schreiber S.L. Org. Lett. 8 (2006) 143
    • (2006) Org. Lett. , vol.8 , pp. 143
    • Taylor, A.M.1    Schreiber, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.