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Volumn 62, Issue 5, 2006, Pages 960-967

α-Amido sulfones from natural α-amino acids and their reaction with carbon nucleophiles

Author keywords

Amino acids; Carbanions; Dipeptides; Imines; Sulfones

Indexed keywords

ACETIC ACID DERIVATIVE; ALDEHYDE DERIVATIVE; AMIDE; AMINO ACID DERIVATIVE; BENZENESULFINIC ACID; CARBON; DIPEPTIDE DERIVATIVE; IMINE; LITHIUM DERIVATIVE; NEF PROTEIN; SULFINIC ACID DERIVATIVE; SULFONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 29144439883     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.10.033     Document Type: Article
Times cited : (11)

References (53)
  • 6
    • 0037043180 scopus 로고    scopus 로고
    • B. List Tetrahedron 58 2002 5573 5590
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 16
    • 0037149691 scopus 로고    scopus 로고
    • α-Hydroxy N-acylamines can be also prepared by oxidative decarboxylation of serine derivatives: (e) D.M. Troast, and J.A. Porco Org. Lett. 4 2002 991 994
    • (2002) Org. Lett. , vol.4 , pp. 991-994
    • Troast, D.M.1    Porco, J.A.2
  • 20
    • 28444474791 scopus 로고    scopus 로고
    • A. Padwa Thieme Stuttgart
    • L. Fišera A. Padwa Science of Synthesis Vol. 27 2004 Thieme Stuttgart 349 373
    • (2004) Science of Synthesis , vol.27 , pp. 349-373
    • Fišera, L.1
  • 37
    • 0346349375 scopus 로고    scopus 로고
    • Aldehydes bearing a cyclic framework as (R)-2,3- isopropylideneglyceraldehyde or (l)-prolinal give the best results in term of diastereoselectivity. On the other hand reaction of N-Boc-phenylalaninal with benzyl carbamate in the presence of benzenesulfinic acid gives the corresponding sulfone in good yield but poor diastereoselectivity: E. Foresti, G. Palmieri, M. Petrini, and R. Profeta Org. Biomol. Chem. 1 2003 4275 4281 See also Ref. 7h
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 4275-4281
    • Foresti, E.1    Palmieri, G.2    Petrini, M.3    Profeta, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.