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Volumn 21, Issue 11-12, 2010, Pages 1382-1388

Asymmetric hydrogenation of trisubstituted N-acetyl enamides derived from 2-tetralones using ruthenium-SYNPHOS catalysts: A practical synthetic approach to the preparation of β3-adrenergic agonist SR58611A

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOTETRALIN DERIVATIVE; [[7 [[2 (3 CHLOROPHENYL) 2 HYDROXYETHYL]AMINO] 5,6,7,8 TETRAHYDRO 2 NAPHTHYL]OXY]ACETIC ACID ETHYL ESTER; AMIDE; KETONE DERIVATIVE; RUTHENIUM COMPLEX;

EID: 77956650129     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2010.03.024     Document Type: Article
Times cited : (25)

References (63)
  • 61
    • 77956651576 scopus 로고    scopus 로고
    • The formyl group of cyclic enamide 2f was removed at room temperature in the presence of 1 equiv of hydrochloric acid in MeOH without racemization, thus providing the corresponding amine in 96% yield and 72% ee
    • The formyl group of cyclic enamide 2f was removed at room temperature in the presence of 1 equiv of hydrochloric acid in MeOH without racemization, thus providing the corresponding amine in 96% yield and 72% ee.
  • 63
    • 77956647324 scopus 로고    scopus 로고
    • The ee was measured for the N-acetylated products obtained after protection of the corresponding amines 3a-d
    • The ee was measured for the N-acetylated products obtained after protection of the corresponding amines 3a-d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.