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Volumn 6, Issue 3-4, 2003, Pages 177-180

Functionalised enones as starting materials for the construction of aziridine scaffolds

Author keywords

Aziridination; Carbamates; Olefination; Scaffold; Solution phase

Indexed keywords

ALPHA KETO ESTER; AZIRIDINE 1,2 DICARBOXYLATE; AZIRIDINE DERIVATIVE; BETA KETO ESTER; DICARBOXYLIC ACID; ESTER DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0346501852     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:MODI.0000006757.23657.11     Document Type: Conference Paper
Times cited : (7)

References (18)
  • 1
    • 0032241286 scopus 로고    scopus 로고
    • Purification of combinatorial libraries
    • Weller, H. N., Purification of combinatorial libraries, Mol. Div., 4 (1999) 47-52.
    • (1999) Mol. Div. , vol.4 , pp. 47-52
    • Weller, H.N.1
  • 2
    • 0034275092 scopus 로고    scopus 로고
    • Methodologies for generating solution-phase combinatorial libraries
    • (a) An, H. and Cook, P. D., Methodologies for generating solution-phase combinatorial libraries, Chem. Rev., 100 (2000) 3311-3340.
    • (2000) Chem. Rev. , vol.100 , pp. 3311-3340
    • An, H.1    Cook, P.D.2
  • 3
    • 0035293182 scopus 로고    scopus 로고
    • Solution- and solid-phase strategies for the design, synthesis, and screening of libraries based on natural product templates: A comprehensive survey
    • (b) Hall, D. C., Manku, S. and Wang, F., Solution- and solid-phase strategies for the design, synthesis, and screening of libraries based on natural product templates: a comprehensive survey, J. Comb. Chem., 3 (2001) 125-150.
    • (2001) J. Comb. Chem. , vol.3 , pp. 125-150
    • Hall, D.C.1    Manku, S.2    Wang, F.3
  • 4
    • 0034796434 scopus 로고    scopus 로고
    • A facile synthesis of N-alkoxycarbonylaziridines from olefins bearing two geminal electron-withdrawing groups
    • (a) Fioravanti, S., Morreale, A., Pellacani, L. and Tardella, P. A., A facile synthesis of N-alkoxycarbonylaziridines from olefins bearing two geminal electron-withdrawing groups, Synthesis, (2001) 1975-1978.
    • (2001) Synthesis , pp. 1975-1978
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 5
    • 0037067548 scopus 로고    scopus 로고
    • Diastereoselective aziridination of chiral β-carbonyl enoates
    • (b) Fioravanti, S., Morreale, A., Pellacani, L. and Tardella, P. A., Diastereoselective aziridination of chiral β-carbonyl enoates, J. Org. Chem., 67 (2002) 4972-4974.
    • (2002) J. Org. Chem. , vol.67 , pp. 4972-4974
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 6
    • 0037424739 scopus 로고    scopus 로고
    • Reagent-controlled diastereoselective aminations with a new chiral nosyloxycarbamate
    • (c) Fioravanti, S., Morreale, A., Pellacani, L. and Tardella, P.A., Reagent-controlled diastereoselective aminations with a new chiral nosyloxycarbamate Tetrahedron Lett., 44 (2003) 3031-3034.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 3031-3034
    • Fioravanti, S.1    Morreale, A.2    Pellacani, L.3    Tardella, P.A.4
  • 7
    • 33847802966 scopus 로고
    • Organoselenium chemistry, conversion of ketones to enones by selenoxide syn elimination
    • Reich, H. J., Renga, J. M. and Reich, I. L., Organoselenium chemistry, conversion of ketones to enones by selenoxide syn elimination, J. Am. Chem. Soc., 97 (1975) 5434-5447.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 5434-5447
    • Reich, H.J.1    Renga, J.M.2    Reich, I.L.3
  • 8
    • 85066110471 scopus 로고
    • A simple route to alkenes having three electron-withdrawing substituents at the double bond
    • Ouali, M. S., Vaultier, M. and Carrié, R., A simple route to alkenes having three electron-withdrawing substituents at the double bond, Synthesis, (1977) 626.
    • (1977) Synthesis , pp. 626
    • Ouali, M.S.1    Vaultier, M.2    Carrié, R.3
  • 9
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C., Finn, M. G. and Sharpless, K. B., Click chemistry: diverse chemical function from a few good reactions, Angew. Chem., Int. Ed. Engl., 40 (2001) 2004-2021.
    • (2001) Angew. Chem., Int. Ed. Engl. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 10
    • 0346369749 scopus 로고    scopus 로고
    • note
    • + < 1), 238 (22), 193 (30), 166 (24), 165 (100), 137 (28), 136 (22), 121 (21), 120 (26).
  • 12
    • 0001848341 scopus 로고
    • The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects
    • Marryanoff, B. E. and Reitz, A. B., The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects, Chem. Rev., 89 (1989) 863-927.
    • (1989) Chem. Rev. , vol.89 , pp. 863-927
    • Marryanoff, B.E.1    Reitz, A.B.2
  • 13
    • 0030977733 scopus 로고    scopus 로고
    • Solid-phase synthesis of peptide mimetics with (E)-alkene amide bond replacements derived from alkenylaziridines
    • Wipf, P. and Henninger, T. C., Solid-phase synthesis of peptide mimetics with (E)-alkene amide bond replacements derived from alkenylaziridines, J. Org. Chem., 62 (1997) 1586-1587.
    • (1997) J. Org. Chem. , vol.62 , pp. 1586-1587
    • Wipf, P.1    Henninger, T.C.2
  • 14
    • 0001706609 scopus 로고
    • New route to diastereomeric (E)-alkene dipeptide isosteres from β-aziridinyl-α, β-enoates by reaction with organocopper reagents
    • Ibuka, T., Nakai, K., Habashita, H., Hotta, Y., Fujii, N., Nimura, N., Miwa, Y., Taga, T. and Yamamoto, Y., New route to diastereomeric (E)-alkene dipeptide isosteres from β-aziridinyl-α, β-enoates by reaction with organocopper reagents, Angew. Chem. 106 (1994), 693-5; Angew. Chem., Int. Ed. Engl., 33 (1994) 652-654.
    • (1994) Angew. Chem. , vol.106 , pp. 693-695
    • Ibuka, T.1    Nakai, K.2    Habashita, H.3    Hotta, Y.4    Fujii, N.5    Nimura, N.6    Miwa, Y.7    Taga, T.8    Yamamoto, Y.9
  • 15
    • 33748237397 scopus 로고
    • Ibuka, T., Nakai, K., Habashita, H., Hotta, Y., Fujii, N., Nimura, N., Miwa, Y., Taga, T. and Yamamoto, Y., New route to diastereomeric (E)-alkene dipeptide isosteres from β-aziridinyl-α, β-enoates by reaction with organocopper reagents, Angew. Chem. 106 (1994), 693-5; Angew. Chem., Int. Ed. Engl., 33 (1994) 652-654.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 652-654
  • 16
    • 0010009889 scopus 로고    scopus 로고
    • Synthesis and aza-[2,3]-Wittig rearrangements of vinylaziridines: Scope and limitations
    • Åhman, J., Jarevång, T. and Somfai, P., Synthesis and aza-[2,3]-Wittig rearrangements of vinylaziridines: scope and limitations, J. Org. Chem., 61 (1996) 8148-8159.
    • (1996) J. Org. Chem. , vol.61 , pp. 8148-8159
    • Åhman, J.1    Jarevång, T.2    Somfai, P.3
  • 17
    • 0030864474 scopus 로고    scopus 로고
    • A highly stereoselective aza-[3,3]-Claisen rearrangement of vinylaziridines as a novel entry to seven-membered lactams
    • Lindström, U. M. and Somfai, P., A highly stereoselective aza-[3,3]-Claisen rearrangement of vinylaziridines as a novel entry to seven-membered lactams, J. Am. Chem. Soc., 119 (1997), 8385-8386.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8385-8386
    • Lindström, U.M.1    Somfai, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.