메뉴 건너뛰기




Volumn 15, Issue 15, 2011, Pages 2658-2672

Organic photochemistry in the construction of heterocyclic compounds

Author keywords

Cycloaddition; Flow chemistry; Heterocycles; Microwave; Photochemistry; Rearrangement

Indexed keywords

ORGANIC COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 79959952053     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211796367273     Document Type: Article
Times cited : (10)

References (69)
  • 1
    • 0003698777 scopus 로고
    • ORGANIC Photochemistry
    • AcademicPress: London
    • Kagan, J. ORGANIC Photochemistry, Principles and Applications; AcademicPress: London, 1993.
    • (1993) Principles and Applications
    • Kagan, J.1
  • 2
    • 42549140767 scopus 로고    scopus 로고
    • Photochemical reactions as key steps in organic synthesis
    • Hoffmann, N. Photochemical reactions as key steps in organic synthesis.Chem. Rev., 2008, 108, 1052-1103.
    • (2008) Chem. Rev , vol.108 , pp. 1052-1103
    • Hoffmann, N.1
  • 3
    • 0037049302 scopus 로고    scopus 로고
    • Ring closure reactions of β-nitroso-, β-acyl-,and β-thiocarbamoyl-α,β-unsaturated sulphilimines. Synthesis of [1,2,5]oxadiazolo [3,4-d]-, isoxazolo [3,4-d]-, and isothiazolo [3,4-d]pyrimidine derivatives from uracils
    • Masahiko, N., Takahashi, M. Ring closure reactions of β-nitroso-, β-acyl-,and β-thiocarbamoyl-α,β-unsaturated sulphilimines. Synthesis of [1,2,5]oxadiazolo [3,4-d]-, isoxazolo [3,4-d]-, and isothiazolo [3,4-d]pyrimidine derivatives from uracils. Tetrahedron, 2002, 58, 10073-10079.
    • (2002) Tetrahedron , vol.58 , pp. 10073-10079
    • Masahiko, N.1    Takahashi, M.2
  • 4
    • 85195239260 scopus 로고    scopus 로고
    • Synthesis of 2H-1,2,3-triazolo [4,5-d]pyrimidine-5,7-diones from uracils using cyclization reaction of β-azo-α,β-unsaturated sulphilimines
    • Masahiko, N., Takahashi, M. Synthesis of 2H-1,2,3-triazolo [4,5-d]pyrimidine-5,7-diones from uracils using cyclization reaction of β-azo-α,β-unsaturated sulphilimines. eterocycles, 2003, 60, 267-684.
    • (2003) Eterocycles , vol.60 , pp. 267-684
    • Masahiko, N.1    Takahashi, M.2
  • 5
    • 0007115033 scopus 로고
    • Shigeru. Thermal and photochemicalCurtius type rearrangement of N-acyl-S,S-diphenylsulphimides
    • Furukawa, N.; Nishio, T.; Fukumara, M.; Shigeru. Thermal and photochemicalCurtius type rearrangement of N-acyl-S,S-diphenylsulphimides. Chem.Lett., 1978, 7, 209-210.
    • (1978) Chem.Lett , vol.7 , pp. 209-210
    • Furukawa, N.1    Nishio, T.2    Fukumara, M.3
  • 6
    • 22144491936 scopus 로고    scopus 로고
    • Synthesis of pyrrolo [2,3-d]pyrimidine-2,4-diones by sunlight photolysis of N-(5-vinyluracil-6-yl) sulphilimines
    • Matsumoto, N.; Takahashi, M. Synthesis of pyrrolo [2,3-d]pyrimidine-2,4-diones by sunlight photolysis of N-(5-vinyluracil-6-yl) sulphilimines. TettrahedronLett., 2005, 46, 5551-5554.
    • (2005) TettrahedronLett , vol.46 , pp. 5551-5554
    • Matsumoto, N.1    Takahashi, M.2
  • 7
  • 8
    • 34547783295 scopus 로고    scopus 로고
    • Synthesis of 1,2,4-Triazolo [3,2-d] benzothiazolesby photolysis of sulphilimines having a methylthio)carbonimidoyl group
    • Takahashi, M.; Satoh, M. Synthesis of 1,2,4-Triazolo [3,2-d] benzothiazolesby photolysis of sulphilimines having a methylthio)carbonimidoyl group. Heterocycles, 2007, 71, 1407-1411.
    • (2007) Heterocycles , vol.71 , pp. 1407-1411
    • Takahashi, M.1    Satoh, M.2
  • 9
    • 43049134074 scopus 로고    scopus 로고
    • Mishra, Synthesis of 2-[4-fluorophenyl]-1,2,4-triazolo [5,1-b] benzothiazoles as antifungal agents
    • Mishra, K.; Wahab, A.; Mishra, Synthesis of 2-[4-fluorophenyl]-1,2,4-triazolo [5,1-b] benzothiazoles as antifungal agents. Ind. J. Heterocycle.Chem., 2007, 17, 183-184.
    • (2007) Ind. J. Heterocycle.Chem , vol.17 , pp. 183-184
    • Mishra, K.1    Wahab, A.2
  • 10
    • 0346339684 scopus 로고    scopus 로고
    • Photochemical synthesisof triazole [3,4-b]1,3(4H)-benzothiazines: A detailed mechanistic studyon photocyclization/photodesulfurisation of triazole-3-thiones
    • Santhilvelan, A.; Thirumalai, D.; Ramakrishman, V.T. Photochemical synthesisof triazole [3,4-b]1,3(4H)-benzothiazines: a detailed mechanistic studyon photocyclization/photodesulfurisation of triazole-3-thiones. Tetrahedron,2004, 60, 851-860.
    • (2004) Tetrahedron , vol.60 , pp. 851-860
    • Santhilvelan, A.1    Thirumalai, D.2    Ramakrishman, V.T.3
  • 12
    • 0036581843 scopus 로고    scopus 로고
    • Synthesis, photochemical synthesis and antitumor evaluation of novel derivativesof thieno [3',2':4,5]thieno [2,3-c]quinolones
    • Dogankoruznjak, J.; Slade, N.; Zamola, B.; Pavelic, K.; Karminski-Zamola, G. Synthesis, photochemical synthesis and antitumor evaluation of novel derivativesof thieno [3',2':4,5]thieno [2,3-c]quinolones. Chem. Pharm. Bull.,2002, 50, 656-660.
    • (2002) Chem. Pharm. Bull , vol.50 , pp. 656-660
    • Dogankoruznjak, J.1    Slade, N.2    Zamola, B.3    Pavelic, K.4    Karminski-Zamola, G.5
  • 13
    • 67649342025 scopus 로고    scopus 로고
    • Photochemical cyclization of thioformanilides by chloranil: An approach to 2-substituted benzothiazoles
    • Rey, V.; Silvia, Soria-Castro, S.M.; Argüello, J.E.; Peñéñory, A.B. Photochemical cyclization of thioformanilides by chloranil: An approach to 2-substituted benzothiazoles. Tetrahedron Lett., 2009, 50, 4720-4723.
    • (2009) Tetrahedron Lett , vol.50 , pp. 4720-4723
    • Rey, V.1    Silvia2    Soria-Castro, S.M.3    Argüello, J.E.4    Peñéñory, A.B.5
  • 14
    • 34547183983 scopus 로고    scopus 로고
    • The photochemical cyclodehydrogenation route topolycyclic azaarenes
    • Hewlins, M.J.E.; Salter, R. The photochemical cyclodehydrogenation route topolycyclic azaarenes. Synthesis, 2007, 2164-217.
    • (2007) Synthesis , pp. 2164-2217
    • Hewlins, M.J.E.1    Salter, R.2
  • 16
    • 65249164455 scopus 로고    scopus 로고
    • Photocyclization of tosyl stilbenes as a key reaction in the preparation of an analogue of the antitumoragent CC-1065
    • Neo, A.G.; Peréz, A.; López, C.; Castedo, L.; Tojo, G. Photocyclization of tosyl stilbenes as a key reaction in the preparation of an analogue of the antitumoragent CC-1065. J. Org. Chem., 2009, 74, 3203-3206.
    • (2009) J. Org. Chem , vol.74 , pp. 3203-3206
    • Neo, A.G.1    Peréz, A.2    López, C.3    Castedo, L.4    Tojo, G.5
  • 17
    • 12344270063 scopus 로고    scopus 로고
    • Photochemicallycatalysed Diels-Alder reaction of arylimines with N-vinylpyrrolidinone andN-vinylcarbazole by 2,4,6-triphenylpyrlium salt: Synthesis of 4-heterocyclesubstitutedtetrahydroquinoline derivatives
    • Zhang, W.; Guo, Y, Liu, Z.; Jin, X.; Yang, Li, Liu, Z-L. Photochemicallycatalysed Diels-Alder reaction of arylimines with N-vinylpyrrolidinone andN-vinylcarbazole by 2,4,6-triphenylpyrlium salt: Synthesis of 4-heterocyclesubstitutedtetrahydroquinoline derivatives. Tetrahedron, 2005, 61, 1325-1333.
    • (2005) Tetrahedron , vol.61 , pp. 1325-1333
    • Zhang, W.1    Guo, Y.2    Liu, Z.3    Jin, X.4    Yang, L.5    Liu, Z.-L.6
  • 18
    • 0032715089 scopus 로고    scopus 로고
    • Generation and capture of iminyl radicals fromketoxime xanthates
    • Gagosz, F.; Zard, S.Z. Generation and capture of iminyl radicals fromketoxime xanthates. Synlett, 1999, 1978-1980.
    • (1999) Synlett , pp. 1978-1980
    • Gagosz, F.1    Zard, S.Z.2
  • 19
    • 0033575448 scopus 로고    scopus 로고
    • Synthesis of dihydropyrroles by the intramolecular additionof alkyideneaminyl radicals generated from O-2,4-dinitrophenyloximes ofγ,δ-unsaturated ketones
    • Uchiyama, K.; Hayashi, Y.; Narasaka, K. Synthesis of dihydropyrroles by the intramolecular additionof alkyideneaminyl radicals generated from O-2,4-dinitrophenyloximes ofγ,δ-unsaturated ketones. Tetrahedron, 1999, 55, 8915-1930.
    • (1999) Tetrahedron , vol.55 , pp. 8915-1930
    • Uchiyama, K.1    Hayashi, Y.2    Narasaka, K.3
  • 20
    • 33747210404 scopus 로고    scopus 로고
    • New lightinducediminyl radical cyclization reactions of acyloximes to isoquinolines
    • Alonso, R.; Campos, P. J.; García, Bábara.; Rodríguez, M. A. New lightinducediminyl radical cyclization reactions of acyloximes to isoquinolines.Org. Lett., 2006, 8, 3521-3523.
    • (2006) Org. Lett , vol.8 , pp. 3521-3523
    • Alonso, R.1    Campos, P.J.2    García, B.3    Rodríguez, M.A.4
  • 21
    • 16244409257 scopus 로고    scopus 로고
    • Photochemical synthesisof benzoxazolo [3,2-b]isoquinolin-11-one and isoquinolino [3,2-b] [1,3]benzoxazin-11-one under basic conditions
    • Senthilvelan, S.; Thirumalai, D.; Ramakrishnan, V.T. Photochemical synthesisof benzoxazolo [3,2-b]isoquinolin-11-one and isoquinolino [3,2-b] [1,3]benzoxazin-11-one under basic conditions. Tetrahedron, 2005, 61,4213-4220.
    • (2005) Tetrahedron , vol.61 , pp. 4213-4220
    • Senthilvelan, S.1    Thirumalai, D.2    Ramakrishnan, V.T.3
  • 22
    • 0037191612 scopus 로고    scopus 로고
    • Heterocycle annulations of enolizable vinyl quinoneimides. Dihydroquinolines and quinolines from thermal 6π-electrocyclizations and indoles from photochemical cyclizations
    • Parker, K.A.; Mindt, T. L. Heterocycle annulations of enolizable vinyl quinoneimides. Dihydroquinolines and quinolines from thermal 6π-electrocyclizations and indoles from photochemical cyclizations. Org. Lett.,2002, 4, 4265-4268.
    • (2002) Org. Lett , vol.4 , pp. 4265-4268
    • Parker, K.A.1    Mindt, T.L.2
  • 23
    • 54049121495 scopus 로고    scopus 로고
    • Highly electron-donating 3,3'-diaryl-1,1'-bi(isobenzofurans)s synthesised by photochemical exocyclic [2+2+2] cycloaddition
    • Zhang, H.; Wakamiya, A.; Yamaguchi, S. Highly electron-donating 3,3'-diaryl-1,1'-bi(isobenzofurans)s synthesised by photochemical exocyclic [2+2+2] cycloaddition. Org. Lett., 2008, 10, 3591-3594.
    • (2008) Org. Lett , vol.10 , pp. 3591-3594
    • Zhang, H.1    Wakamiya, A.2    Yamaguchi, S.3
  • 24
    • 0242504005 scopus 로고    scopus 로고
    • Synthetic principles for bandgap control in linear π-conjugatedsystems
    • Roncali, J. Synthetic principles for bandgap control in linear π-conjugatedsystems. Chem. Rev., 1997, 97, 173-206.
    • (1997) Chem. Rev , vol.97 , pp. 173-206
    • Roncali, J.1
  • 25
    • 0036214613 scopus 로고    scopus 로고
    • Recent advances in the stereocontrolled synthesisof bi- and tricyclic β-lactams with non-classical structure
    • Alcaide, B.; Almendros, P. Recent advances in the stereocontrolled synthesisof bi- and tricyclic β-lactams with non-classical structure. Curr. Org. Chem.,2002, 6, 245-264.
    • (2002) Curr. Org. Chem , vol.6 , pp. 245-264
    • Alcaide, B.1    Almendros, P.2
  • 27
    • 10744223326 scopus 로고    scopus 로고
    • Design and synthesis of pyrrolidine-5,5'-trans-lactams (5-oxo-hexahydropyrrolo [3,2-b]pyrroles) as novel mechanism-based inhibitorsof human cytomegalovirus protease.4. Antiviral activity and plasma stability
    • Borthwick, A.D.; Davies, D.E.; Ertl, P.F.; Exall, A.M.; Haley, T.M.; Hart, G.J.; Jackson, D.L.; Parry, N.R.; Patikis, A.; Trivedi, N.; Weingarten, G.G.; Woolven, J.M. Design and synthesis of pyrrolidine-5,5'-trans-lactams (5-oxo-hexahydropyrrolo [3,2-b]pyrroles) as novel mechanism-based inhibitorsof human cytomegalovirus protease.4. Antiviral activity and plasma stability. J. Med. Chem., 2003, 46, 4428-4449.
    • (2003) J. Med. Chem , vol.46 , pp. 4428-4449
    • Borthwick, A.D.1    Davies, D.E.2    Ertl, P.F.3    Exall, A.M.4    Haley, T.M.5    Hart, G.J.6    Jackson, D.L.7    Parry, N.R.8    Patikis, A.9    Trivedi, N.10    Weingarten, G.G.11    Woolven, J.M.12
  • 28
    • 27644594831 scopus 로고    scopus 로고
    • Proteasome inhibition by a totally synthetic -lactamrelated to salinosporamide A aand omuralide
    • Hogan, P.; Corey, E.J. Proteasome inhibition by a totally synthetic -lactamrelated to salinosporamide A aand omuralide. J. Am. Chem. Soc., 2005, 127,15386-15387.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 15386-15387
    • Hogan, P.1    Corey, E.J.2
  • 29
    • 37049092557 scopus 로고
    • Synthetic routes to -lactams
    • Isaacs, S. N. Synthetic routes to -lactams. Chem. Soc. Rev., 1976, 5, 181-202.
    • (1976) Chem. Soc. Rev , vol.5 , pp. 181-202
    • Isaacs, S.N.1
  • 31
    • 0000776232 scopus 로고
    • Cyclopropanone- -lactamsconversions via hydroxylamines
    • Wasserman, H.H.; Glazer, E.A.; Hearm, M.J. Cyclopropanone- -lactamsconversions via hydroxylamines. Tetrahedron Lett., 1973, 14, 4855-4858.
    • (1973) Tetrahedron Lett , vol.14 , pp. 4855-4858
    • Wasserman, H.H.1    Glazer, E.A.2    Hearm, M.J.3
  • 32
    • 37648999551 scopus 로고    scopus 로고
    • Synthesis and photoreactivity of some 5-alkylidene- and 5-alkylidenamine-2, 5-dihydroisoxazoles
    • Donati, D.; Fusi, S.; Ponticelli, F.; Paccani, R.R. Synthesis and photoreactivity of some 5-alkylidene- and 5-alkylidenamine-2, 5-dihydroisoxazoles. Tetrahedron Lett., 2008, 49, 764-767.
    • (2008) Tetrahedron Lett , vol.49 , pp. 764-767
    • Donati, D.1    Fusi, S.2    Ponticelli, F.3    Paccani, R.R.4
  • 33
    • 0345171711 scopus 로고    scopus 로고
    • Photochemical synthesis of a 4,5-dihydrofuroazetidinone, a novel -lactam system
    • Donati, D.; Fusi, S.; Ponticelli, F. Photochemical synthesis of a 4,5-dihydrofuroazetidinone, a novel -lactam system. Tetrahedron Lett., 2003,44, 9247-9250.
    • (2003) Tetrahedron Lett , vol.44 , pp. 9247-9250
    • Donati, D.1    Fusi, S.2    Ponticelli, F.3
  • 34
    • 33846098692 scopus 로고    scopus 로고
    • Photoreaction of some 5-alkylidene-2,5-dihydroisoxazoles: Facile contruction of novelun classical -lactam containing heterocycles
    • Donati, D.; Fusi, S.; Ponticelli, F.; Paccani, R.R.; Adamo, F. A. Photoreaction of some 5-alkylidene-2,5-dihydroisoxazoles: facile contruction of novelun classical -lactam containing heterocycles. Tetrahedron, 2007, 63, 1583-1588.
    • (2007) Tetrahedron , vol.63 , pp. 1583-1588
    • Donati, D.1    Fusi, S.2    Ponticelli, F.3    Paccani, R.R.4    Adamo, F.A.5
  • 35
    • 0034740923 scopus 로고    scopus 로고
    • Diazoketones as precursors in -lactam synthesis. New insights into the mechanism of the photochemically induced Staudinger reaction
    • Linder, M.R.; Frey, W.U. Diazoketones as precursors in -lactam synthesis. New insights into the mechanism of the photochemically induced Staudinger reaction. J. Chem. Soc. Perkin. 1, 2001, 2566-2577.
    • (2001) J. Chem. Soc. Perkin , vol.1 , pp. 2566-2577
    • Linder, M.R.1    Frey, W.U.2
  • 36
    • 33646544385 scopus 로고    scopus 로고
    • Origin of the relative stereochemistry of the -lactam formation in the Staudinger reaction
    • Jiao, L.; Liang, Y.; Xu, J. Origin of the relative stereochemistry of the -lactam formation in the Staudinger reaction. J. Am. Chem. Soc., 2006, 128,6060-6069.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 6060-6069
    • Jiao, L.1    Liang, Y.2    Xu, J.3
  • 38
    • 42649131714 scopus 로고    scopus 로고
    • Asymmetric synthesis of -lactams using chiral-memory effect on photochemical -hydrogen abstractionby thicarbonyl group
    • Sakamoto, M.; Kawanishi, H.; Mino, T.; Fujita, T. Asymmetric synthesis of -lactams using chiral-memory effect on photochemical -hydrogen abstractionby thicarbonyl group. Chem. Commun., 2008, 2132-2133.
    • (2008) Chem. Commun , pp. 2132-2133
    • Sakamoto, M.1    Kawanishi, H.2    Mino, T.3    Fujita, T.4
  • 39
    • 0037007725 scopus 로고    scopus 로고
    • Controlof enantioselectivity in the photochemical conversion of oxoamides into -lactam derivatives
    • Natarajan, A.; Wang, K.; Ramamurthy, V.; Scheffer, J.R.; Patrick, B. Controlof enantioselectivity in the photochemical conversion of oxoamides into -lactam derivatives. Org. Lett., 2002, 4, 1443-1446.
    • (2002) Org. Lett , vol.4 , pp. 1443-1446
    • Natarajan, A.1    Wang, K.2    Ramamurthy, V.3    Scheffer, J.R.4    Patrick, B.5
  • 40
    • 1242307350 scopus 로고    scopus 로고
    • B-lactam-forming photochemicalreactions of N-trimethylsilylmethyl- and N-tributylstannylmethyl substituted α-ketoamides
    • Wang, R.; Chen, C.; Duesler, E.; Mariano, P.S. B-lactam-forming photochemicalreactions of N-trimethylsilylmethyl- and N-tributylstannylmethyl substituted α-ketoamides. J. Org. Chem., 2004, 69, 1215-1220.
    • (2004) J. Org. Chem , vol.69 , pp. 1215-1220
    • Wang, R.1    Chen, C.2    Duesler, E.3    Mariano, P.S.4
  • 41
    • 0142026571 scopus 로고    scopus 로고
    • Rearrangements of bicyclicnitrones to lactams: Comparison of photochemical and modified Bartonconditions
    • Zeng, Y.; Smith, B.T.; Hershberger, J.; Aub, J. Rearrangements of bicyclicnitrones to lactams: comparison of photochemical and modified Bartonconditions.J. Org. Chem., 2003, 68, 8065-8067.
    • (2003) J. Org. Chem , vol.68 , pp. 8065-8067
    • Zeng, Y.1    Smith, B.T.2    Hershberger, J.3    Aub, J.4
  • 42
    • 0343371530 scopus 로고    scopus 로고
    • Formation of lactamsvia photoelectron-transfer catalysed reactions of N-allylamines with α, β-unsaturated ester
    • Das, S.; Dileep, J.S.; Shivaramayya, K.; George, M.V. Formation of lactamsvia photoelectron-transfer catalysed reactions of N-allylamines with α, β-unsaturated ester. Tetrahedron, 1996, 52, 3425-3434.
    • (1996) Tetrahedron , vol.52 , pp. 3425-3434
    • Das, S.1    Dileep, J.S.2    Shivaramayya, K.3    George, M.V.4
  • 43
    • 7744232650 scopus 로고    scopus 로고
    • Indolizidine and quinolizidine alkaloids
    • Michael, J. P. Indolizidine and quinolizidine alkaloids. Nat. Prod. Rep., 2004,21, 625-649.
    • (2004) Nat. Prod. Rep , vol.21 , pp. 625-649
    • Michael, J.P.1
  • 44
    • 85195237592 scopus 로고
    • Hoffmann-La Roche & Co. 3-hydroxypyrrolidin-2-one derivatives, process and intermediates for theirpreparation and pharmaceutical preparations containing them
    • Patent0071216, February 9
    • Ascwanden, W.; Kyburz, E. Hoffmann-La Roche & Co. 3-hydroxypyrrolidin-2-one derivatives, process and intermediates for theirpreparation and pharmaceutical preparations containing them. Europ. Patent0071216, February 9, 1983.
    • (1983) Europ
    • Ascwanden, W.1    Kyburz, E.2
  • 45
    • 34047266642 scopus 로고    scopus 로고
    • An efficientand highly stereoselective method to synthesise 3-(1-hydroxyalkyl)pyrrolidinone
    • Lian, G-Y.; Yu, J-D.; Yang, H-F.; Lin, F.; Gao, Q.; Zhang, D-W. An efficientand highly stereoselective method to synthesise 3-(1-hydroxyalkyl)pyrrolidinone. Chem. Lett., 2007,36, 408-409.
    • (2007) Chem. Lett , vol.36 , pp. 408-409
    • Lian, G.-Y.1    Yu, J.-D.2    Yang, H.-F.3    Lin, F.4    Gao, Q.5    Zhang, D.-W.6
  • 46
    • 18744400583 scopus 로고    scopus 로고
    • Photochemical synthesis of N substituted 3-hydroxy-2-pyrrolidinones
    • Obkircher, M.; Seufert, S.; Giese, B. Photochemical synthesis of N substituted 3-hydroxy-2-pyrrolidinones. Synlett, 2005, 1182-1184.
    • (2005) Synlett , pp. 1182-1184
    • Obkircher, M.1    Seufert, S.2    Giese, B.3
  • 47
    • 85195237421 scopus 로고    scopus 로고
    • Preparation of arylpyrrolidines as inhibitors of cyclic amp-specific phophodiesterase and as inhibitors of tumor necrosis factor release
    • U.S patent 6423710B1, July 23
    • Martins, T. J.; Fowler, K.W.; Odingo, J.; Kesicki, E.A.; Oliver, A.; Burgess, L.E.; Gaudino, J.J.; Jones, Z.S.; Newhouse, B.J.; Schlachter, S.T. Preparation of arylpyrrolidines as inhibitors of cyclic AMP-specific phophodiesterase and as inhibitors of tumor necrosis factor release. U.S patent 6423710B1,July 23, 2002.
    • (2002)
    • Martins, T.J.1    Fowler, K.W.2    Odingo, J.3    Kesicki, E.A.4    Oliver, A.5    Burgess, L.E.6    Gaudino, J.J.7    Jones, Z.S.8    Newhouse, B.J.9    Schlachter, S.T.10
  • 48
    • 34047266642 scopus 로고    scopus 로고
    • An efficient and highly stereo selective method to synthesise 3-(1-hydroxyalkyl) pyrrolidinone
    • Lian, G-Y.; Yu, J-D.; Yang, H-F.; Lin, F.; Gao, Q.; Zhang, D-W. An efficient and highly stereo selective method to synthesise 3-(1-hydroxyalkyl) pyrrolidinone. Chem. Lett., 2007, 36, 408-409.
    • (2007) Chem. Lett , vol.36 , pp. 408-409
    • Lian, G.-Y.1    Yu, J.-D.2    Yang, H.-F.3    Lin, F.4    Gao, Q.5    Zhang, D.-W.6
  • 49
    • 33845324113 scopus 로고    scopus 로고
    • Photochemical synthesis ofisomeric (E/Z)-3-alkylidene-3H-isobenzofuranones
    • Mor, S.; Dhawan, S. N.; Kapoor, M; Munar, D. Photochemical synthesis ofisomeric (E/Z)-3-alkylidene-3H-isobenzofuranones. Tetrahedron, 2007, 63,594-597.
    • (2007) Tetrahedron , vol.63 , pp. 594-597
    • Mor, S.1    Dhawan, S.N.2    Kapoor, M.3    Munar, D.4
  • 53
    • 56349121618 scopus 로고    scopus 로고
    • New 6-oxa-2-silabicyclo [2.2.0]hexanes by photochemical conversion of acyl(allyl)(dimethyl)silanes
    • Hammaecher, C.; Portella, C. New 6-oxa-2-silabicyclo [2.2.0]hexanes by photochemical conversion of acyl(allyl)(dimethyl)silanes. Chem. Commun.2008, 5833-5835,
    • (2008) Chem. Commun , pp. 5833-5835
    • Hammaecher, C.1    Portella, C.2
  • 54
    • 71049133485 scopus 로고    scopus 로고
    • The effects of Homoharring-tonine in patients with cronic myeloid leukemia who have failed or responded suboptimally to imatinib therapy
    • Z, J-B
    • Li, Y-F.; Liu, X.; Liu, D-S.; Din, B-H.; Z, J-B. The effects of Homoharring-tonine in patients with cronic myeloid leukemia who have failed or responded suboptimally to imatinib therapy. Leukemia Lymphoma, 2009, 50,1889-1891.
    • (2009) Leukemia Lymphoma , vol.50 , pp. 1889-1891
    • Li, Y.-F.1    Liu, X.2    Liu, D.-S.3    Din, B.-H.4
  • 55
    • 0037432905 scopus 로고    scopus 로고
    • A rapid stereo controlled entry to the ABCD tetracyclic core of neotuberostemonine
    • Booker-Milburn, K. I.; Hirst, P.; Charmant, J.P.H.; Taylor, L.H.J. A rapid stereo controlled entry to the ABCD tetracyclic core of neotuberostemonine. Angew. Chem. Int. Ed, 2003, 42, 1642-1644.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 1642-1644
    • Booker-Milburn, K.I.1    Hirst, P.2    Charmant, J.P.H.3    Taylor, L.H.J.4
  • 56
    • 36348974535 scopus 로고    scopus 로고
    • Acid-catalysed rearrangement of fused alkylideneoxetanols
    • Hickford, P.J.; Baker, J.R.; Bruce, I.; Booker-Milburn, K. I. Acid-catalysed rearrangement of fused alkylideneoxetanols, Org. Lett, 2007, 9, 4681-4684.
    • (2007) Org. Lett , vol.9 , pp. 4681-4684
    • Hickford, P.J.1    Baker, J.R.2    Bruce, I.3    Booker-Milburn, K.I.4
  • 57
    • 77950982518 scopus 로고    scopus 로고
    • Photochemical rearrangement of N-chlorolactams: A route to N-heterocycles through concerted ring contraction
    • Winter, D.K.; Drouin, A.; Lessard, J.; Spino, C. Photochemical rearrangement of N-chlorolactams: A route to N-heterocycles through concerted ring contraction. J. Org. Chem., 2010, 75, 2610-2618.
    • (2010) J. Org. Chem , vol.75 , pp. 2610-2618
    • Winter, D.K.1    Drouin, A.2    Lessard, J.3    Spino, C.4
  • 59
    • 33646463152 scopus 로고    scopus 로고
    • Tandem photocycloaddition-retro-Mannich fragmentation of enaminones. A route to spiropyrrolines and the tetracyclic core of Koumine
    • White, J.D.; Ihle, D.C. Tandem photocycloaddition-retro-Mannich fragmentation of enaminones. A route to spiropyrrolines and the tetracyclic core of Koumine. Org. Lett., 2006, 8, 1081-1084.
    • (2006) Org. Lett , vol.8 , pp. 1081-1084
    • White, J.D.1    Ihle, D.C.2
  • 60
    • 68149144261 scopus 로고    scopus 로고
    • Spiropyran as a selective, sensitive, and reproducible cyanide anion receptor
    • Shiraishi, Y.; Adachi, K.; Itoh, M.; Hirai, T. Spiropyran as a selective, sensitive,and reproducible cyanide anion receptor. Org. Lett., 2009, 11, 3482-3485.
    • (2009) Org. Lett , vol.11 , pp. 3482-3485
    • Shiraishi, Y.1    Adachi, K.2    Itoh, M.3    Hirai, T.4
  • 61
    • 77953138778 scopus 로고    scopus 로고
    • Flow chemistry using milli- and microstructured reactors-from conventional to novel process windows
    • Illg, T.; Löd, P.; Hessel, V. Flow chemistry using milli- and microstructured reactors-from conventional to novel process windows. Bioorg. Med. Chem.,2010, 18, 3707-3719.
    • (2010) Bioorg. Med. Chem , vol.18 , pp. 3707-3719
    • Illg, T.1    Löd, P.2    Hessel, V.3
  • 63
    • 76549092999 scopus 로고    scopus 로고
    • Current methods for characterising mixing and flow in micro channels
    • Aubin J.; Ferrando, M.; Jiricny, V. Current methods for characterising mixing and flow in micro channels. Chem. Eng. Sci., 2010, 65, 2065-2093.
    • (2010) Chem. Eng. Sci , vol.65 , pp. 2065-2093
    • Aubin, J.1    Ferrando, M.2    Jiricny, V.3
  • 65
    • 51549106272 scopus 로고    scopus 로고
    • A protecting group free synthesis of (±)-Neostenine via the [5+2] photocyclo addition of Maleimides
    • Lainchbury, M.D.; Medlet, M.I.; Taylor, P.M.; Hirst, P.; Dohle, W.; Booker-Milburn, K.I. A protecting group free synthesis of (±)-Neostenine via the [5+2] photocyclo addition of Maleimides. J. Org. Chem., 2008, 73, 6497-6505.
    • (2008) J. Org. Chem , vol.73 , pp. 6497-6505
    • Lainchbury, M.D.1    Medlet, M.I.2    Taylor, P.M.3    Hirst, P.4    Dohle, W.5    Booker-Milburn, K.I.6
  • 66
    • 55149094086 scopus 로고    scopus 로고
    • Micro-photochemistry: Photochemistry in microstructured reactors. The newphotochemistry of the future
    • Coyle, E.E.; Oelgemöller, M. Micro-photochemistry: photochemistry in microstructured reactors. The newphotochemistry of the future. Photochem. Photobiol. Sci., 2008, 7, 1313-1322.
    • (2008) Photochem. Photobiol. Sci , vol.7 , pp. 1313-1322
    • Coyle, E.E.1    Oelgemöller, M.2
  • 67
    • 55149098643 scopus 로고    scopus 로고
    • Intramolecular photocyclization of 2-(2-alkenyloxymethyl)-naphthalene-1-carbonitriles using glassmade Microreactors
    • Mukae, H.; Maeda, H.; Nashihara, S.; Mizuno, K. Intramolecular photocyclization of 2-(2-alkenyloxymethyl)-naphthalene-1-carbonitriles using glassmade Microreactors. Bull. Chem. Soc. Jpn., 2007, 80, 1157-1161.
    • (2007) Bull. Chem. Soc. Jpn , vol.80 , pp. 1157-1161
    • Mukae, H.1    Maeda, H.2    Nashihara, S.3    Mizuno, K.4
  • 68
    • 67650863398 scopus 로고    scopus 로고
    • Microwave photocatalysis II: Novelcontinuous-flow microwave photocatalytic experiments set-up with titaniacoated mercury electrodeless discharge lamps
    • Žabová, H.; Církva, Z.; Hájek, M. Microwave photocatalysis II: novelcontinuous-flow microwave photocatalytic experiments set-up with titaniacoated mercury electrodeless discharge lamps. J. Chem. Technol. Biotechnol.,2009, 84, 1125-1129.
    • (2009) J. Chem. Technol. Biotechnol , vol.84 , pp. 1125-1129
    • Žabová, H.1    Církva, Z.2    Hájek, M.3
  • 69
    • 75149192819 scopus 로고    scopus 로고
    • Microwave photocatalysis V: Low pressure batch and continuous-flow microwavephotoreactors with quartz mercury electrodeless discharge lamps. Photohydrolysis of monchloroacetic acid
    • Žabová, H.; Církva, Z.; Relich, S.; Hájek, M. Microwave photocatalysis V: low pressure batch and continuous-flow microwavephotoreactors with quartz mercury electrodeless discharge lamps. Photohydrolysis of monchloroacetic acid. J. Chem. Technol. Biotechnol.,2010, 85, 185-191.
    • (2010) J. Chem. Technol. Biotechnol , vol.85 , pp. 185-191
    • Žabová, H.1    Církva, Z.2    Relich, S.3    Hájek, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.