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Volumn 65, Issue 19, 2000, Pages 6160-6166

Solid-phase synthesis of 1,2,3,4-tetrahydro-2-pyridones via aza-annulation of enamines

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3,4 TETRAHYDRO 2 PYRIDONE DERIVATIVE; ACID ANHYDRIDE; ACRYLIC ACID DERIVATIVE; AMINE; ENAMINE; HETEROCYCLIC COMPOUND; KETONE; PYRIDONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034703198     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000676c     Document Type: Article
Times cited : (49)

References (93)
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    • Balasubramanian, M.1    Keay, J.G.2
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    • MDL Drug Data Registry
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    • 0041678498 scopus 로고    scopus 로고
    • Anaheim, CA.; March ORGN 226
    • th ACS National Meeting, Anaheim, CA.; March 1999, ORGN 226.
    • (1999) th ACS National Meeting
  • 76
    • 0003148146 scopus 로고
    • Trost, B. M., Ed.; Pergamon Press: Oxford
    • (a) Jung, M. E. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 4, pp 1-67.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1-67
    • Jung, M.E.1
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    • Treatment of the enamino amide 12a with 4 equiv of 13a or 13b under the annulation reaction conditions provided the corresponding aza-annulation products 14a and 14b in good yields and purity. In this study, the enamino amide 12a was prepared by treating 10 with 4 equiv of 11a
    • Treatment of the enamino amide 12a with 4 equiv of 13a or 13b under the annulation reaction conditions provided the corresponding aza-annulation products 14a and 14b in good yields and purity. In this study, the enamino amide 12a was prepared by treating 10 with 4 equiv of 11a.
  • 89
    • 0343778360 scopus 로고    scopus 로고
    • In a solution phase study, reaction of tert-butyl enamino amide, prepared from N-benzylpropynoic amide and 25 equiv of tert-butylamine, with 13a provided the corresponding aza-annulation product only in 28% yield
    • In a solution phase study, reaction of tert-butyl enamino amide, prepared from N-benzylpropynoic amide and 25 equiv of tert-butylamine, with 13a provided the corresponding aza-annulation product only in 28% yield.
  • 93
    • 0343342702 scopus 로고    scopus 로고
    • 13C NMR data without purification
    • 13C NMR data without purification.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.