A concise and traceless linker strategy toward combinatorial libraries of 2,6,9-substituted purines

[1] Adams J L, 1999, Curr Opin Drug Discov Devel, V2, P96

[2] PREPARATION AND APPLICATION OF THE 5-(4-(9-FLUORENYLMETHYLOXYCARBONYL)AMINOMETHYL-3,5-DIMETHOXYPHENOXY)VALERIC ACID (PAL) HANDLE FOR THE SOLID-PHASE SYNTHESIS OF C-TERMINAL PEPTIDE AMIDES UNDER MILD CONDITIONS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (12) : 3730 - 3743

[3] Solid-phase synthesis of 1,4-benzodiazepine-2,5-diones. Library preparation and demonstration of synthesis generality [J]. JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (05) : 1240 - 1256

[4] Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors [J]. CHEMISTRY & BIOLOGY, 1999, 6 (06): : 361 - 375

[5] The development and therapeutic potential of protein kinase inhibitors [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (04) : 459 - 465

[6] REGIOSPECIFIC ALKYLATION OF 6-CHLOROPURINE AND 2,6-DICHLOROPURINE AT N7 BY TRANSIENT PROTECTION OF N3/N9 BY METHYLCOBALOXIME [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (12): : 1696 - 1697

[7] Novel solid-phase preparation of 2,6,9-trisubstituted purines for combinatorial library generation [J]. TETRAHEDRON LETTERS, 2001, 42 (15) : 2771 - 2773

[8] Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells [J]. NATURE MEDICINE, 1996, 2 (05) : 561 - 566

[9] García-Echeverría C, 2000, MED RES REV, V20, P28, DOI 10.1002/(SICI)1098-1128(200001)20:1<28::AID-MED2>3.0.CO

[10] 2-2

[1] Adams J L, 1999, Curr Opin Drug Discov Devel, V2, P96

[2] PREPARATION AND APPLICATION OF THE 5-(4-(9-FLUORENYLMETHYLOXYCARBONYL)AMINOMETHYL-3,5-DIMETHOXYPHENOXY)VALERIC ACID (PAL) HANDLE FOR THE SOLID-PHASE SYNTHESIS OF C-TERMINAL PEPTIDE AMIDES UNDER MILD CONDITIONS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (12) : 3730 - 3743

[3] Solid-phase synthesis of 1,4-benzodiazepine-2,5-diones. Library preparation and demonstration of synthesis generality [J]. JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (05) : 1240 - 1256

[4] Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors [J]. CHEMISTRY & BIOLOGY, 1999, 6 (06): : 361 - 375

[5] The development and therapeutic potential of protein kinase inhibitors [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (04) : 459 - 465

[6] REGIOSPECIFIC ALKYLATION OF 6-CHLOROPURINE AND 2,6-DICHLOROPURINE AT N7 BY TRANSIENT PROTECTION OF N3/N9 BY METHYLCOBALOXIME [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (12): : 1696 - 1697

[7] Novel solid-phase preparation of 2,6,9-trisubstituted purines for combinatorial library generation [J]. TETRAHEDRON LETTERS, 2001, 42 (15) : 2771 - 2773

[8] Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells [J]. NATURE MEDICINE, 1996, 2 (05) : 561 - 566

[9] García-Echeverría C, 2000, MED RES REV, V20, P28, DOI 10.1002/(SICI)1098-1128(200001)20:1<28::AID-MED2>3.0.CO

[10] 2-2