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Volumn 17, Issue 16, 2006, Pages 2366-2376

Nitrile biotransformations for the practical synthesis of highly enantiopure azido carboxylic acids and amides, 'click' to functionalized chiral triazoles and chiral β-amino acids

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; CARBOXYLIC ACID DERIVATIVE; NITRILE; NITRILE HYDRATASE; PHENYLACETYLENE; PROPIONIC ACID DERIVATIVE;

EID: 33749255560     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.08.021     Document Type: Article
Times cited : (24)

References (75)
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    • For a review of 'click' chemistry in drug discovery, see:
    • For a review of 'click' chemistry in drug discovery, see:. Kolb H.C., and Sharpless K.B. Drug Discovery Today 8 (2003) 128
    • (2003) Drug Discovery Today , vol.8 , pp. 128
    • Kolb, H.C.1    Sharpless, K.B.2
  • 14
    • 0004295295 scopus 로고
    • Patai S. (Ed), Interscience, London
    • In: Patai S. (Ed). The Chemistry of the Azido Group (1971), Interscience, London
    • (1971) The Chemistry of the Azido Group
  • 15
    • 0003590357 scopus 로고
    • Supplement D., Patai S., and Rappoport Z. (Eds), Wiley, Chichester
    • In: Supplement D., Patai S., and Rappoport Z. (Eds). The Chemistry of Halides, Pseudo-Halides, and Azides (1983), Wiley, Chichester
    • (1983) The Chemistry of Halides, Pseudo-Halides, and Azides
  • 24
    • 0004289338 scopus 로고
    • Lwowski W. (Ed), Interscience, New York
    • In: Lwowski W. (Ed). Nitrenes (1970), Interscience, New York
    • (1970) Nitrenes
  • 29
    • 17844376761 scopus 로고    scopus 로고
    • For a useful review, see:
    • For a useful review, see:. Eguchi S. ARKIVOC part 2 (2005) 98
    • (2005) ARKIVOC , vol.PART 2 , pp. 98
    • Eguchi, S.1
  • 30
    • 18444392425 scopus 로고    scopus 로고
    • For recent examples, see:
    • For recent examples, see:. Gil C., and Bräse S. Chem. Eur. J. 11 (2005) 2680
    • (2005) Chem. Eur. J. , vol.11 , pp. 2680
    • Gil, C.1    Bräse, S.2
  • 33
    • 0033920416 scopus 로고    scopus 로고
    • For a review of catalytic asymmetric ring opening reaction of epoxides by an azide, see:
    • For a review of catalytic asymmetric ring opening reaction of epoxides by an azide, see:. Jacobsen E.N. Acc. Chem. Res. 33 (2000) 421
    • (2000) Acc. Chem. Res. , vol.33 , pp. 421
    • Jacobsen, E.N.1
  • 34
    • 14944358971 scopus 로고    scopus 로고
    • For a review of catalytic asymmetric addition reactions of azide to α,β-unsaturated compounds, see:
    • For a review of catalytic asymmetric addition reactions of azide to α,β-unsaturated compounds, see:. Xu L.-W., and Xia C.-G. Eur. J. Org. Chem. (2005) 633
    • (2005) Eur. J. Org. Chem. , pp. 633
    • Xu, L.-W.1    Xia, C.-G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.