AAAAAA

   
Results: 1-25 | 26-41
Results: 1-25/41
Tris (perfluoroalkylethyl)silyl alkyl amines as calibration standards for electron ionization mass spectrometry in the mass range of 100-3000 Da
Authors: Fishman, VN Linclau, B Curran, DP Somayajula, KV
Citation: Vn. Fishman et al., Tris (perfluoroalkylethyl)silyl alkyl amines as calibration standards for electron ionization mass spectrometry in the mass range of 100-3000 Da, J AM SOC M, 12(9), 2001, pp. 1050-1054
Synthesis and asymmetric hydrogermylation reactions of dithiogermanium hydrides derived from C2-symmetric dithiols
Authors: Curran, DP Gualtieri, G
Citation: Dp. Curran et G. Gualtieri, Synthesis and asymmetric hydrogermylation reactions of dithiogermanium hydrides derived from C2-symmetric dithiols, SYNLETT, 2001, pp. 1038-1041
Fluorous reverse phase silica gel. A new tool for preparative separations in synthetic organic and organofluorine chemistry
Authors: Curran, DP
Citation: Dp. Curran, Fluorous reverse phase silica gel. A new tool for preparative separations in synthetic organic and organofluorine chemistry, SYNLETT, (9), 2001, pp. 1488-1496
Semi-fluorinated trialkyltin fluorides and fluorinated telechelic ionomersas viscosity-enhancing agents for carbon dioxide
Authors: Shi, CM Huang, ZH Beckman, EJ Enick, RM Kim, SY Curran, DP
Citation: Cm. Shi et al., Semi-fluorinated trialkyltin fluorides and fluorinated telechelic ionomersas viscosity-enhancing agents for carbon dioxide, IND ENG RES, 40(3), 2001, pp. 908-913
The highly lipophilic DNA topoisomerase I inhibitor DB-67 displays elevated lactone levels in human blood and potent anticancer activity
Authors: Bom, D Curran, DP Zhang, J Zimmer, SG Bevins, R Kruszewski, S Howe, JN Bingcang, A Latus, LJ Burke, TG
Citation: D. Bom et al., The highly lipophilic DNA topoisomerase I inhibitor DB-67 displays elevated lactone levels in human blood and potent anticancer activity, J CONTR REL, 74(1-3), 2001, pp. 325-333
Synthesis of perfluorinated allylic compounds by radical allylation and their purification over fluorous reverse-phase silica
Authors: Ryu, IY Kreimerman, S Niguma, T Minakata, S Komatsu, M Luo, ZY Curran, DP
Citation: Iy. Ryu et al., Synthesis of perfluorinated allylic compounds by radical allylation and their purification over fluorous reverse-phase silica, TETRAHEDR L, 42(5), 2001, pp. 947-950
Thiol additions to acrylates by fluorous mixture synthesis: relative control of elution order in demixing by the fluorous tag and the thiol substituent
Authors: Curran, DP Oderaotoshi, Y
Citation: Dp. Curran et Y. Oderaotoshi, Thiol additions to acrylates by fluorous mixture synthesis: relative control of elution order in demixing by the fluorous tag and the thiol substituent, TETRAHEDRON, 57(24), 2001, pp. 5243-5253
Fluorous mixture synthesis: A fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds
Authors: Luo, ZY Zhang, QS Oderaotoshi, Y Curran, DP
Citation: Zy. Luo et al., Fluorous mixture synthesis: A fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds, SCIENCE, 291(5509), 2001, pp. 1766-1769
Fluorous Boc ((F)Boc) carbamates: New amine protecting groups for use in fluorous synthesis
Authors: Luo, ZY Williams, J Read, RW Curran, DP
Citation: Zy. Luo et al., Fluorous Boc ((F)Boc) carbamates: New amine protecting groups for use in fluorous synthesis, J ORG CHEM, 66(12), 2001, pp. 4261-4266
Fluorous triphasic reactions: Transportative deprotection of fluorous silyl ethers with concomitant purification
Authors: Nakamura, H Linclau, B Curran, DP
Citation: H. Nakamura et al., Fluorous triphasic reactions: Transportative deprotection of fluorous silyl ethers with concomitant purification, J AM CHEM S, 123(41), 2001, pp. 10119-10120
Switching enantiofacial selectivities using one chiral source: Catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones
Authors: Yabu, K Masumoto, S Yamasaki, S Hamashima, Y Kanai, M Du, W Curran, DP Shibasaki, M
Citation: K. Yabu et al., Switching enantiofacial selectivities using one chiral source: Catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones, J AM CHEM S, 123(40), 2001, pp. 9908-9909
Synthesis of enantioenriched axially chiral anilides from atropisomerically enriched tartarate ortho-anilides
Authors: Ates, A Curran, DP
Citation: A. Ates et Dp. Curran, Synthesis of enantioenriched axially chiral anilides from atropisomerically enriched tartarate ortho-anilides, J AM CHEM S, 123(21), 2001, pp. 5130-5131
Solution phase synthesis of libraries of polycyclic natural product analogue by cascade radical annulation: Synthesis of a 64-member library of mappicine analogues and a 48-member library of mappicine ketone analogues
Authors: de Frutos, O Curran, DP
Citation: O. De Frutos et Dp. Curran, Solution phase synthesis of libraries of polycyclic natural product analogue by cascade radical annulation: Synthesis of a 64-member library of mappicine analogues and a 48-member library of mappicine ketone analogues, J COMB CHEM, 2(6), 2000, pp. 639-649
Selective sulfonylation of 1,2-diols and derivatives catalyzed by a recoverable fluorous tin oxide
Authors: Bucher, B Curran, DP
Citation: B. Bucher et Dp. Curran, Selective sulfonylation of 1,2-diols and derivatives catalyzed by a recoverable fluorous tin oxide, TETRAHEDR L, 41(49), 2000, pp. 9617-9621
Asymmetric alkylation of aromatic aldehydes with diethylzinc catalyzed by a fluorous BINOL-Ti complex in an organic and fluorous biphase system
Authors: Nakamura, Y Takeuchi, S Ohgo, Y Curran, DP
Citation: Y. Nakamura et al., Asymmetric alkylation of aromatic aldehydes with diethylzinc catalyzed by a fluorous BINOL-Ti complex in an organic and fluorous biphase system, TETRAHEDR L, 41(1), 2000, pp. 57-60
Preparation of a fluorous chiral BINOL derivative and application to an asymmetric protonation reaction
Authors: Nakamura, Y Takeuchi, S Ohgo, Y Curran, DP
Citation: Y. Nakamura et al., Preparation of a fluorous chiral BINOL derivative and application to an asymmetric protonation reaction, TETRAHEDRON, 56(3), 2000, pp. 351-356
Fluorous methods for synthesis and separation of organic molecules
Authors: Curran, DP
Citation: Dp. Curran, Fluorous methods for synthesis and separation of organic molecules, PUR A CHEM, 72(9), 2000, pp. 1649-1653
Round trip radical reactions from acyclic precursors to tricyclo[5.3.1.0(2,6)]undecanes. A new cascade radical cyclization approach to (+/-)-isogymnomitrene and (+/-)-gymnomitrene
Authors: Haney, BP Curran, DP
Citation: Bp. Haney et Dp. Curran, Round trip radical reactions from acyclic precursors to tricyclo[5.3.1.0(2,6)]undecanes. A new cascade radical cyclization approach to (+/-)-isogymnomitrene and (+/-)-gymnomitrene, J ORG CHEM, 65(7), 2000, pp. 2007-2013
Separation of "light fluorous" reagents and catalysts by fluorous solid-phase extraction: Synthesis and study of a family of triarylphosphines bearing linear and branched fluorous tags
Authors: Zhang, QS Luo, ZY Curran, DP
Citation: Qs. Zhang et al., Separation of "light fluorous" reagents and catalysts by fluorous solid-phase extraction: Synthesis and study of a family of triarylphosphines bearing linear and branched fluorous tags, J ORG CHEM, 65(26), 2000, pp. 8866-8873
The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity
Authors: Bom, D Curran, DP Kruszewski, S Zimmer, SG Strode, JT Kohlhagen, G Du, W Chavan, AJ Fraley, KA Bingcang, AL Latus, LJ Pommier, Y Burke, TG
Citation: D. Bom et al., The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity, J MED CHEM, 43(21), 2000, pp. 3970-3980
On the reduction of tertiary radicals by samarium diiodide (SmI2)
Authors: Nagashima, T Rivkin, A Curran, DP
Citation: T. Nagashima et al., On the reduction of tertiary radicals by samarium diiodide (SmI2), CAN J CHEM, 78(6), 2000, pp. 791-799
Highlights from two decades of synthetic radical chemistry
Authors: Curran, DP
Citation: Dp. Curran, Highlights from two decades of synthetic radical chemistry, ALDRICHIM A, 33(3), 2000, pp. 104-110
Experimental techniques in fluorous synthesis: a user's guide
Authors: Curran, DP Hadida, S Studer, A He, M Kim, SY Luo, ZY Larhed, M Hallberg, A Linclau, B
Citation: Dp. Curran et al., Experimental techniques in fluorous synthesis: a user's guide, PRACT APPR, 233, 2000, pp. 327-352
Determination of the absolute configuration of 1,3,5,7-tetramethyl-1,3-dihydroindol-2-one by optical rotation computation
Authors: Kondru, RK Chen, CHT Curran, DP Beratan, DN Wipf, P
Citation: Rk. Kondru et al., Determination of the absolute configuration of 1,3,5,7-tetramethyl-1,3-dihydroindol-2-one by optical rotation computation, TETRAHEDR-A, 10(21), 1999, pp. 4143-4150
Enantioselective conjugate radical addition reactions mediated by chiral Lewis acid complexes of (R,R)-4,6-dibenzofurandiyl-2,2 '-bis(4-phenyloxazoline) (DBFOX/Ph)
Authors: Iserloh, U Curran, DP Kanemasa, S
Citation: U. Iserloh et al., Enantioselective conjugate radical addition reactions mediated by chiral Lewis acid complexes of (R,R)-4,6-dibenzofurandiyl-2,2 '-bis(4-phenyloxazoline) (DBFOX/Ph), TETRAHEDR-A, 10(12), 1999, pp. 2417-2428
Risultati: 1-25 | 26-41