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Volumn 63, Issue 51, 2007, Pages 12740-12746

Synthesis of the octahydroindole unit of aeruginosins via asymmetric hydrogenation of the Diels-Alder adducts of 2-amido-2,4-pentadienoate

Author keywords

[No Author keywords available]

Indexed keywords

2 AMIDO 2,4 PENTADIENOATE; INDOLE DERIVATIVE; METHYL 2 ACETAMIDO 2,4 PENTADIENOATE DERIVATIVE; OCTAHYDROINDOLE; UNCLASSIFIED DRUG;

EID: 35748978556     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.09.078     Document Type: Article
Times cited : (7)

References (32)
  • 27
    • 35748981052 scopus 로고    scopus 로고
    • note
    • The asymmetric hydrogenation of 9aA utilizing a rhodium catalyst [Rh-DuPHOS] resulted in a complex mixture.
  • 30
    • 35748977018 scopus 로고    scopus 로고
    • note
    • The reaction in methanol resulted in the formation of dimethyl acetal of 12.
  • 32
    • 35748939883 scopus 로고    scopus 로고
    • note
    • Acid isomerization of its methyl ester was demonstrated by Bonjoch et al. (see Ref 8b). It was explained that the equilibrium is due to acid-mediated β-elimination of the β-amino ketone, vinylogous enolization, and intramolecular Michael readdition.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.