메뉴 건너뛰기




Volumn 60, Issue 5, 2004, Pages 1107-1124

A direct link between the Passerini reaction and α-lactams

Author keywords

Aziridinones; Maleic anhydride; Mono and dicarboxylic acids; Nucleophilic substitution; Passerini reaction

Indexed keywords

1 (1 ADAMANTYL) 3 TERT BUTYLAZIRIDINONE; 1 (1 ADAMANTYL) 3,3 DIMETHYLAZIRIDINONE; 1 TERT BUTYL 3,3 DIMETHYLAZIRIDINONE; 1,3 DI TERT BUTYLAZIRIDINONE; 2 (1 ADAMANTYL) 2 (2,2 DIMETHYLPROPANOLOXY) 2 METHYLPROPANAMIDE; AMIDE; AZIRIDINE DERIVATIVE; BIS(2 METHYL N TERT BUTYLPROPANAMIDO 2)MALEATE; CARBOXYLIC ACID DERIVATIVE; DICARBOXYLIC ACID DERIVATIVE; LACTAM DERIVATIVE; N (1 ADAMANTYL) 2 ACETOXY 2 METHYLPROPANAMIDE; N (1 ADAMANTYL) 2 ACETOXY 3,3 DIMETHYLBUTANAMIDE; N (1 ADAMANTYL) 2 BENZOLOYLOXY 3,3 DIMETHYLBUTANAMIDE; N (1 ADAMANTYL) 2 BENZOYLOXY 2 METHYLPROPANAMIDE; N (1 ADAMANTYL) 2 METHYL 2 (3 PHENYLACRYLOYLOXY)PROPANAMIDE; N (1 ADAMANTYL) 2 METHYL 2 TRIFLUOROACETOXYPROPANAMIDE; N (1 ADAMANTYL) 3,3 DIMETHYL 2 (2,2 DIMETHYLPROPANOYLOXY)BUTANAMIDE; N (1 ADAMANTYL) 3,3 DIMETHYL 2 (3 PHENYLACRYLOYLOXY)BUTANAMIDE; N TERT BUTYL 2 (2,2 DIMETHYLPROPANOYLOXY) 2 METHYLPROPANAMIDE; N TERT BUTYL 2 ACETOXY 2 METHYLPROPANAMIDE; N TERT BUTYL 2 ACETOXY 3,3 DIMETHYLBUTANAMIDE; N TERT BUTYL 2 BENZOYLOXY 2 METHYLPROPANAMIDE; N TERT BUTYL 2 BENZOYLOXY 3,3 DIMETHYLBUTANAMIDE; N TERT BUTYL 2 METHYL 2 (3 PHENYLACRYLOYLOXY)PROPANAMIDE; N TERT BUTYL 2 METHYL 2 TRIFLUOROACETOXYPROPANAMIDE; N TERT BUTYL 3,3 DIMETHYL 2 (2,2 DIMETHYLPROPANOYLOXY)BUTANAMIDE; N TERT BUTYL 3,3 DIMETHYL 2 (3 PHENYLACRYLOYLOXY)BUTANAMIDE; N TERT BUTYL 3,3 DIMETHYL 2 TRIFLUOROACETOXYBUTANAMIDE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 0347600547     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.11.067     Document Type: Article
Times cited : (16)

References (44)
  • 7
    • 0004270887 scopus 로고
    • The Passerini reaction and related reactions
    • I. Ugi. New York: Academic
    • Marquarding D., Gokel G., Hoffmann P., Ugi I. The Passerini reaction and related reactions. Ugi I. Isonitrile chemistry. 1971;133-143 Academic, New York.
    • (1971) Isonitrile Chemistry , pp. 133-143
    • Marquarding, D.1    Gokel, G.2    Hoffmann, P.3    Ugi, I.4
  • 9
    • 0028757621 scopus 로고
    • Multicomponent reactions in organic chemistry
    • Ugi I., Dömling A., Hörl W. Multicomponent reactions in organic chemistry. Endeavour. 18:1994;115-122.
    • (1994) Endeavour , vol.18 , pp. 115-122
    • Ugi, I.1    Dömling, A.2    Hörl, W.3
  • 10
    • 0001855113 scopus 로고
    • also Angew. Chem., Int. Ed. 1968, 7, 25-36
    • Lengyel I., Sheehan J.C. Angew. Chem. 80:1968;27-37. also Angew. Chem., Int. Ed. 1968, 7, 25-36.
    • (1968) Angew. Chem. , vol.80 , pp. 27-37
    • Lengyel, I.1    Sheehan, J.C.2
  • 25
    • 0346356226 scopus 로고
    • also Angew. Chem., Int. Ed. 1968, 7, 894-895
    • Bott K. Angew. Chem. 80:1968;970-971. also Angew. Chem., Int. Ed. 1968, 7, 894-895.
    • (1968) Angew. Chem. , vol.80 , pp. 970-971
    • Bott, K.1
  • 30
    • 0038801722 scopus 로고
    • 8)andanα-lactam(5)intermediatehavebeenpostulatedinaPasserini- likereaction,nofirmevidencehasbeenprovided: Although both an imino-oxirane (
    • Although both an imino-oxirane ( 8 ) and an α-lactam ( 5 ) intermediate have been postulated in a Passerini-like reaction, no firm evidence has been provided: Saegusa T., Taka-ishi N., Fujii H. Tetrahedron. 24:1968;3795-3798.
    • (1968) Tetrahedron , vol.24 , pp. 3795-3798
    • Saegusa, T.1    Taka-Ishi, N.2    Fujii, H.3
  • 36
    • 0001427691 scopus 로고
    • see also pp 741-754; also, Angew. Chem., Int. Ed. 1963, 2, 565-598 and 633-645
    • Huisgen R. Angew. Chem. 75:1963;604-637. see also pp 741-754; also, Angew. Chem., Int. Ed. 1963, 2, 565-598 and 633-645.
    • (1963) Angew. Chem. , vol.75 , pp. 604-637
    • Huisgen, R.1
  • 37
    • 0000093806 scopus 로고
    • also, Angew. Chem., Int. Ed. 1968, 7, 321-328
    • Huisgen R. Angew. Chem. 80:1968;329-336. also, Angew. Chem., Int. Ed. 1968, 7, 321-328.
    • (1968) Angew. Chem. , vol.80 , pp. 329-336
    • Huisgen, R.1
  • 38
    • 0001640615 scopus 로고
    • 1976, 41, 403-419
    • Huisgen R. J. Org. Chem. 33:1968;2291-2297. 1976, 41, 403-419.
    • (1968) J. Org. Chem. , vol.33 , pp. 2291-2297
    • Huisgen, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.