메뉴 건너뛰기




Volumn 39, Issue 12, 2009, Pages 2108-2115

Solid-phase synthesis of N-aryl succinimides

Author keywords

Silica bound benzoyl chloride; solid phase synthesis; succinimide

Indexed keywords

BENZYL DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; SILICON DIOXIDE; SUCCINIMIDE DERIVATIVE;

EID: 67650264041     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802638529     Document Type: Article
Times cited : (15)

References (32)
  • 1
    • 0003744388 scopus 로고    scopus 로고
    • Czarnik, A. W, Ed, Wiley: New York
    • Czarnik, A. W. (Ed.) Solid-Phase Organic Synthesis; Wiley: New York, 2001.
    • (2001) Solid-Phase Organic Synthesis
  • 2
    • 0036436990 scopus 로고    scopus 로고
    • Solid-phase heterocyclic chemistry
    • Krchnak, V.; Holladay, M. W. Solid-phase heterocyclic chemistry. Chem. Rev. 2002, 102, 61-91.
    • (2002) Chem. Rev , vol.102 , pp. 61-91
    • Krchnak, V.1    Holladay, M.W.2
  • 3
    • 0036628561 scopus 로고    scopus 로고
    • Traceless solid-phase organic synthesis
    • Blaney, P.; Grigg, R.; Sridharan, V. Traceless solid-phase organic synthesis. Chem. Rev. 2002, 102, 2607-2624.
    • (2002) Chem. Rev , vol.102 , pp. 2607-2624
    • Blaney, P.1    Grigg, R.2    Sridharan, V.3
  • 4
    • 0041037814 scopus 로고    scopus 로고
    • Recent advances in the preparation of heterocycles on solid support
    • Franzén, R. G. Recent advances in the preparation of heterocycles on solid support. J. Comb. Chem. 2000, 2, 195-214.
    • (2000) J. Comb. Chem , vol.2 , pp. 195-214
    • Franzén, R.G.1
  • 5
    • 4944221253 scopus 로고    scopus 로고
    • Comprehensive survey of combinatorial library synthesis
    • Dolle, R. E. Comprehensive survey of combinatorial library synthesis. J. Comb. Chem. 2004, 6, 623-679.
    • (2004) J. Comb. Chem , vol.6 , pp. 623-679
    • Dolle, R.E.1
  • 7
    • 0033683359 scopus 로고    scopus 로고
    • Linkers and cleavage strategies in solid- phase organic synthesis and combinatorial chemistry
    • Guillier, F.; Orain, D.; Bradley, M. Linkers and cleavage strategies in solid- phase organic synthesis and combinatorial chemistry. Chem. Rev. 2000, 100, 2091-2157.
    • (2000) Chem. Rev , vol.100 , pp. 2091-2157
    • Guillier, F.1    Orain, D.2    Bradley, M.3
  • 8
    • 0346527675 scopus 로고    scopus 로고
    • H.-Y. Mei, and A. W. Czarnik, Eds, Marcel Dekker: New York
    • Lebl, M. In Integrated Drug Discovery Technologies; H.-Y. Mei, and A. W. Czarnik, (Eds.); Marcel Dekker: New York, 2002; 395-405.
    • (2002) Integrated Drug Discovery Technologies , pp. 395-405
    • Lebl, M.1
  • 10
    • 0004127585 scopus 로고    scopus 로고
    • Nicolaou, K. C, Hanko, R, Hartwig, W, Eds, Wiley-VCH: Weinheim, vols
    • Nicolaou, K. C.; Hanko, R.; Hartwig, W. (Eds.) Handbook of Combinatorial Chemistry; Wiley-VCH: Weinheim, 2002; vols. 1-2.
    • (2002) Handbook of Combinatorial Chemistry , vol.1-2
  • 11
    • 9644280906 scopus 로고    scopus 로고
    • Investigations into the utility of high-surface-area silica pellets as potential solid-phase synthesis supports
    • Timofte, R. S.; Titman, J. J.; Shao, L.; Stephens, J. C.; Woodward, S. Investigations into the utility of high-surface-area silica pellets as potential solid-phase synthesis supports. Tetrahedron 2005, 61, 51-59.
    • (2005) Tetrahedron , vol.61 , pp. 51-59
    • Timofte, R.S.1    Titman, J.J.2    Shao, L.3    Stephens, J.C.4    Woodward, S.5
  • 12
    • 0041634254 scopus 로고
    • Functionalized silica gel as a support for solid-phase organic synthesis
    • Keana, J. F. W.; Shimizu, M.; Jernstedt, K. K. Functionalized silica gel as a support for solid-phase organic synthesis. J. Org. Chem. 1986, 51, 1641-1644.
    • (1986) J. Org. Chem , vol.51 , pp. 1641-1644
    • Keana, J.F.W.1    Shimizu, M.2    Jernstedt, K.K.3
  • 13
    • 0001222391 scopus 로고
    • Piperazino-functionalized silica gel as a deblocking-scavenging agent for the 9-fluorenylmethyloxycar- bonyl amino-protecting group
    • Carpino, L. A.; Mansour, E. M. E.; Knapczyk, J. Piperazino-functionalized silica gel as a deblocking-scavenging agent for the 9-fluorenylmethyloxycar- bonyl amino-protecting group. J. Org. Chem. 1983, 48, 666-669.
    • (1983) J. Org. Chem , vol.48 , pp. 666-669
    • Carpino, L.A.1    Mansour, E.M.E.2    Knapczyk, J.3
  • 14
    • 13644262196 scopus 로고    scopus 로고
    • An efficient construction of bridged chiral tetracyclic indolidines, a core structure of asperparaline, via stereocontrolled catalytic Pauson-Khand reaction
    • Tanimori, S.; Sunami, T.; Fukubayashi, K.; Kirihata, M. An efficient construction of bridged chiral tetracyclic indolidines, a core structure of asperparaline, via stereocontrolled catalytic Pauson-Khand reaction. Tetrahedron 2005, 61, 2481-2492.
    • (2005) Tetrahedron , vol.61 , pp. 2481-2492
    • Tanimori, S.1    Sunami, T.2    Fukubayashi, K.3    Kirihata, M.4
  • 15
    • 0242467655 scopus 로고    scopus 로고
    • Synthesis of the first monoaromatic B-ring B-azasteroid ring system by sequential angular annulation
    • Marson, C. M.; Pink, J. H.; Smith, C. Synthesis of the first monoaromatic B-ring B-azasteroid ring system by sequential angular annulation. Tetrahedron 2003, 59, 10019-10023.
    • (2003) Tetrahedron , vol.59 , pp. 10019-10023
    • Marson, C.M.1    Pink, J.H.2    Smith, C.3
  • 18
    • 0030969782 scopus 로고    scopus 로고
    • Synthesis and x-ray crystallographic structure of leucine-phenylalanyl succinimide-based pseudopeptides
    • Abell, A. D.; Oldham, M. D. Synthesis and x-ray crystallographic structure of leucine-phenylalanyl succinimide-based pseudopeptides. J. Org. Chem. 1997, 62, 1509-1513.
    • (1997) J. Org. Chem , vol.62 , pp. 1509-1513
    • Abell, A.D.1    Oldham, M.D.2
  • 20
    • 0031562105 scopus 로고    scopus 로고
    • Regioselecive reduction of various 3-aminosuccinimides: Application to the synthesis of two heterocyclic systems
    • Briere, J.-F.; Charpentier, P.; Dupas, G.; Queguiner, G.; Bourguignon, J. Regioselecive reduction of various 3-aminosuccinimides: Application to the synthesis of two heterocyclic systems. Tetrahedron 1997, 53, 2075-2086.
    • (1997) Tetrahedron , vol.53 , pp. 2075-2086
    • Briere, J.-F.1    Charpentier, P.2    Dupas, G.3    Queguiner, G.4    Bourguignon, J.5
  • 21
    • 0030982682 scopus 로고    scopus 로고
    • Lewis acid and hexamethyldi- silazane-promoted efficient synthesis of N-alkyl- and N-arylimide derivatives
    • Reddy, P. Y.; Kondo, S.; Toru, T.; Ueno, Y. Lewis acid and hexamethyldi- silazane-promoted efficient synthesis of N-alkyl- and N-arylimide derivatives. J. Org. Chem. 1997, 62, 2652-2654.
    • (1997) J. Org. Chem , vol.62 , pp. 2652-2654
    • Reddy, P.Y.1    Kondo, S.2    Toru, T.3    Ueno, Y.4
  • 22
    • 3142580903 scopus 로고    scopus 로고
    • Synthesis of 3,3-diarylpyrrolidines from diaryl ketones
    • Katritzky, A. R.; Nair, S. K.; Witek, R. M.; Hutchins, S. M. Synthesis of 3,3-diarylpyrrolidines from diaryl ketones. Arkivoc 2003, 5, 9-18.
    • (2003) Arkivoc , vol.5 , pp. 9-18
    • Katritzky, A.R.1    Nair, S.K.2    Witek, R.M.3    Hutchins, S.M.4
  • 23
    • 0041330319 scopus 로고    scopus 로고
    • Asymmetric synthesis of 5-arylmethylpyrrolidin-2-ones and 2-arylmethylpyrrolidines
    • Lebrun, S.; Couture, A.; Deniau, E.; Grandclaudon, P. Asymmetric synthesis of 5-arylmethylpyrrolidin-2-ones and 2-arylmethylpyrrolidines. Tetrahedron: Asymmetry 2003, 14, 2625-2632.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 2625-2632
    • Lebrun, S.1    Couture, A.2    Deniau, E.3    Grandclaudon, P.4
  • 24
    • 33846597076 scopus 로고    scopus 로고
    • A practical method for the synthesis of pyrrolizidine, indolizidine, and pyrroloazepinolizidine nucleus
    • Quiroz, T.; Corona, D.; Covarruvias, A.; Avila-Zarraga, J. G.; Romero- Ortega, M. A practical method for the synthesis of pyrrolizidine, indolizidine, and pyrroloazepinolizidine nucleus. Tetrahedron Lett. 2007, 48, 1571-1575.
    • (2007) Tetrahedron Lett , vol.48 , pp. 1571-1575
    • Quiroz, T.1    Corona, D.2    Covarruvias, A.3    Avila-Zarraga, J.G.4    Romero- Ortega, M.5
  • 26
    • 29144524966 scopus 로고    scopus 로고
    • Cyanuric chloride: Decent dehydrating agent for an exclusive and efficient synthesis of kinetically controlled isomaleimides
    • Haval, K. P.; Mhaske, S. B.; Argade, N. P. Cyanuric chloride: Decent dehydrating agent for an exclusive and efficient synthesis of kinetically controlled isomaleimides. Tetrahedron 2006, 62, 937-942.
    • (2006) Tetrahedron , vol.62 , pp. 937-942
    • Haval, K.P.1    Mhaske, S.B.2    Argade, N.P.3
  • 27
    • 0028145274 scopus 로고
    • Deoxygenation of sulfoxides with silica chloride
    • Mohanazadeh, F.; Momeni, A. R.; Ranjbar, Y. Deoxygenation of sulfoxides with silica chloride. Tetrahedron Lett. 1994, 35, 6127-6128.
    • (1994) Tetrahedron Lett , vol.35 , pp. 6127-6128
    • Mohanazadeh, F.1    Momeni, A.R.2    Ranjbar, Y.3
  • 28
    • 0344442254 scopus 로고    scopus 로고
    • Silica chloride: A versatile heterogeneous catalyst for esterification and transesterification
    • Srinivas, K. V. N. S.; Mahender, I.; Das, B. Silica chloride: A versatile heterogeneous catalyst for esterification and transesterification. Synthesis 2003, 2390-2394.
    • (2003) Synthesis , pp. 2390-2394
    • Srinivas, K.V.N.S.1    Mahender, I.2    Das, B.3
  • 29
    • 0942278916 scopus 로고    scopus 로고
    • Silica chloride/ wet SiO2 as a novel heterogeneous system for the deprotection of acetals under mild conditions
    • Mirjalili, B.; Pourjavadi, A.; Zolfigol, M. A.; Bamoniri, A. Silica chloride/ wet SiO2 as a novel heterogeneous system for the deprotection of acetals under mild conditions. Phosphorus, Sulfur Silicon Relat. Elem. 2003, 178, 2667-2670.
    • (2003) Phosphorus, Sulfur Silicon Relat. Elem , vol.178 , pp. 2667-2670
    • Mirjalili, B.1    Pourjavadi, A.2    Zolfigol, M.A.3    Bamoniri, A.4
  • 30
    • 33745076725 scopus 로고    scopus 로고
    • An efficient method for the esterification ofamino acids using silica chloride
    • Sathe, M.; Kaushik, M. P. An efficient method for the esterification ofamino acids using silica chloride. Catal. Commun. 2006, 7, 644-646.
    • (2006) Catal. Commun , vol.7 , pp. 644-646
    • Sathe, M.1    Kaushik, M.P.2
  • 31
    • 33845374912 scopus 로고
    • Selective protection of carbonyl compounds: Silica gel treated with thionyl chloride as an effective catalyst for thioacetalization
    • Kamitori, Y.; Hojo, M.; Masuda, R.; Kimura, T.; Yoshida, T. Selective protection of carbonyl compounds: Silica gel treated with thionyl chloride as an effective catalyst for thioacetalization. J. Org. Chem. 1986, 51, 1427-1431.
    • (1986) J. Org. Chem , vol.51 , pp. 1427-1431
    • Kamitori, Y.1    Hojo, M.2    Masuda, R.3    Kimura, T.4    Yoshida, T.5
  • 32
    • 67650270511 scopus 로고    scopus 로고
    • Maatschappij, N. V. Imides. Belg. 1963, 623, 333; Chem. Abstr. 1964, 60, 9157d.
    • Maatschappij, N. V. Imides. Belg. 1963, 623, 333; Chem. Abstr. 1964, 60, 9157d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.