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Volumn 4, Issue 17, 2002, Pages 2913-2916

Total synthesis of the alkaloids martinelline and martinellic acid via a hetero Diels-Alder multicomponent coupling reaction

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBENZOIC ACID; 4 AMINOBENZOIC ACID DERIVATIVE; 4 AMINOBENZOIC ACID METHYL ESTER; ALKALOID; ANTIINFECTIVE AGENT; BRADYKININ RECEPTOR; GUANIDINE; MARTINELLIC ACID; MARTINELLINE; METHYL 4-AMINOBENZOATE; PYRROLE DERIVATIVE; PYRROLINE; QUINOLINE DERIVATIVE;

EID: 0012815011     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026293d     Document Type: Article
Times cited : (194)

References (39)
  • 18
    • 84872272356 scopus 로고    scopus 로고
    • note
    • 1a and 1b have binding affinities toward guinea pig bradykinin B2 of >25 and 10 mg/mL, respectively.
  • 22
    • 0000354729 scopus 로고
    • and references cited therein
    • Povarov, L. S. Russ. Chem. Rev. 1967, 36, 656-670 and references cited therein.
    • (1967) Russ. Chem. Rev. , vol.36 , pp. 656-670
    • Povarov, L.S.1
  • 23
    • 0035813377 scopus 로고    scopus 로고
    • Subsequent to this report, two other groups have reported similar reactions
    • (a) Batey, R. A.; Powell, D. A.; Acton, A.; Lough, A. J. Tetrahedron Lett. 2001, 42, 7935-7939. Subsequent to this report, two other groups have reported similar reactions.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 7935-7939
    • Batey, R.A.1    Powell, D.A.2    Acton, A.3    Lough, A.J.4
  • 26
    • 84872276167 scopus 로고    scopus 로고
    • note
    • The endo- and exo-diastereomers are defined based on the Diels-Alder reaction where H-4 and H-3a have a cis and trans relationship, respectively.
  • 27
    • 84872263409 scopus 로고    scopus 로고
    • note
    • 2" reactions, for instance, in which one component reacts in a similar manner (e.g., diacylation of a diamine). Further discussions on the classification of these types of reactions will be the subject of a future paper.
  • 35
    • 0000255490 scopus 로고
    • In accord with earlier observations, we have found that the Troc group in not stable to hydrogenation; however, deprotection of the Cbz groups occurs faster than the Troc group, and if the reaction is carefully monitored, adequate yields of 5 can be obtained. Hancock, G.; Galpin, I. J.; Morgan, B. A. Tetrahedron Lett. 1982, 23, 249-252.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 249-252
    • Hancock, G.1    Galpin, I.J.2    Morgan, B.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.