메뉴 건너뛰기




Volumn 46, Issue 49, 2005, Pages 8471-8474

Catalyst-free multicomponent Strecker reaction in acetonitrile

Author keywords

Aldehydes; Amines; Aminonitriles; Multicomponent reactions; Strecker reaction

Indexed keywords

ACETONITRILE; ALDEHYDE; ALIPHATIC AMINE; AMINONITRILE; AROMATIC AMINE; CYANIDE; LEWIS ACID; NITRILE; SOLVENT; TRIMETHYLSILYL CYANIDE; UNCLASSIFIED DRUG;

EID: 27644482318     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.10.020     Document Type: Article
Times cited : (84)

References (38)
  • 4
    • 0344451844 scopus 로고    scopus 로고
    • G. Helmchen R.W. Hoffmann J. Mulzer Thieme Stuttgart
    • H. Kunz G. Helmchen R.W. Hoffmann J. Mulzer Stereoselective Synthesis (Houben-Weyl) Vol. 3 1996 Thieme Stuttgart 1931 1952
    • (1996) Stereoselective Synthesis (Houben-Weyl) , vol.3 , pp. 1931-1952
    • Kunz, H.1
  • 7
    • 33746470627 scopus 로고    scopus 로고
    • S.-I. Murahashi Thieme Stuttgart
    • M. North S.-I. Murahashi Science of Synthesis Vol. 19 2004 Thieme Stuttgart 285 310
    • (2004) Science of Synthesis , vol.19 , pp. 285-310
    • North, M.1
  • 33
    • 4644225402 scopus 로고    scopus 로고
    • For a review, see: E. Alessio Chem. Rev. 104 2004 4203 4242
    • (2004) Chem. Rev. , vol.104 , pp. 4203-4242
    • Alessio, E.1
  • 34
    • 27644513881 scopus 로고    scopus 로고
    • note
    • 4 and the solvents were removed under reduced pressure to give in many cases the pure α-aminonitrile (for compounds with yields higher than 95%). In some cases, the aforementioned residues had to be chromatographied using silica gel and mixtures of hexane/ethyl acetate of increasing polarity in order to obtain the pure α-aminonitrile products. Yields are included in Figures 1 and 2, Table 1 and Scheme 2.
  • 38
    • 27644524893 scopus 로고    scopus 로고
    • note
    • This alternative mechanistic pathway was kindly suggested by a referee. We thank her/him for that.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.