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Volumn 4, Issue 26, 2002, Pages 4575-4578

New and Efficient Synthesis of Azabicyclo[4.4.0]alkane Amino Acids by Rh-Catalyzed Cyclohydrocarbonylation

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; CYCLOPEPTIDE; DIPEPTIDE; FUSED HETEROCYCLIC RINGS; HETEROCYCLIC COMPOUND; RHODIUM;

EID: 0141826237     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026782d     Document Type: Article
Times cited : (34)

References (15)
  • 13
    • 0000195595 scopus 로고
    • Jackson et al. reported a facile bicyclization of an alkenyldiamine under classical hydroformylation conditions. This reaction is likely to proceed thorough an iminium ion intermediate. See: Campi, E. M.; Jackson, W. R.; McCubbin, Q. J.; Trnacek, A. E. Aust. J. Chem. 1994, 47, 1061-1070.
    • (1994) Aust. J. Chem. , vol.47 , pp. 1061-1070
    • Campi, E.M.1    Jackson, W.R.2    McCubbin, Q.J.3    Trnacek, A.E.4
  • 14
    • 0442266638 scopus 로고    scopus 로고
    • note
    • 2. The autoclave was immersed into an oil bath that was maintained at 60-65°C and kept for 20 h with magnetic stirring. Then, the autoclave was cooled to room temperature and pressure was slowly released. Solvent was evaporated to give a viscous oil, which was purified by flash chromatography on silica gel to give 5.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.