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340

CC(C)(C)[Si](OCC1CC(N)C1O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)(c1ccccc1)c1ccccc1
Reaction #6058
title compound
収率 184.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCC1CC(Nc2nc(N)nc(O)c2[N+](=O)[O-])C1O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)(c1ccccc1)c1ccccc1
Reaction #6059
title compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CN(c2ccncc2NC(=O)c2nc(Br)c(F)cc2N)CC[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #157114
trans-(+/−)-tert-butyl 1-(3-(3-amino-6-bromo-5-fluoropicolinamido)pyridin-4-yl)-4-(tert-butyldimethylsilyloxy)piperidin-3-yl-carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CN(c2ccncc2NC(=O)c2ccc(F)c(Br)n2)CC[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #157174
tert-butyl (3R,4R)-1-(3-(6-bromo-5-fluoropicolinamido)pyridin-4-yl)-4-(tert-butyldimethylsilyloxy)piperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1C[C@@H](O[Si](C)(C)C(C)(C)C)CN(c2ccncc2NC(=O)c2nc(Br)ccc2N)C1
Reaction #157176
tert-butyl (3S,5R)-1-(3-(3-amino-6-bromopicolinamido)pyridin-4-yl)-5-(tert-butyldimethylsilyloxy)piperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CNC[C@H](F)C1
Reaction #160721
(3R,5R)-3-(tert-butyldimethylsilyloxy)-5-fluoropiperidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NCC2NCCCC2O[Si](C)(C)C(C)(C)C)ccc(C#N)c1Cl
Reaction #204925
DOI: 10.1039/C8SC04228D
CC(Cc1cccc(CC(=O)NC2CCCCCC2)c1)NCC(O)c1ccc(O)c(CO)c1
Reaction #205113
DOI: 10.1039/C8SC04228D
COC(=O)Cc1cccc(CC(C)NCC(O[Si](C)(C)C(C)(C)C)c2ccc(OCc3ccccc3)c3[nH]c(=O)ccc23)c1
Reaction #205656
DOI: 10.1039/C8SC04228D
COCCCOc1cc(CC(CC(NC(=O)OC(C)(C)C)C(CC(C(=O)NCc2ccccc2)C(C)C)O[Si](C)(C)C(C)(C)C)C(C)C)ccc1OC
Reaction #211738
DOI: 10.1039/C8SC04228D
Cc1c(NC(c2nnc(-c3ccccc3)s2)C(C)O)ccc(C#N)c1Cl
Reaction #226404
DOI: 10.1039/C8SC04228D
CC(C)N(CCC(c1ccccc1)c1cc(CCCCOc2ccc(CCNCC(O[Si](C)(C)C(C)(C)C)c3ccc(O)c4[nH]c(=O)ccc34)cc2)ccc1O)C(C)C
Reaction #239387
DOI: 10.1039/C8SC04228D
CC(Cc1cccc(CC(=O)O)c1)NCC(O[Si](C)(C)C(C)(C)C)c1ccc(O)c(CO)c1
Reaction #243587
DOI: 10.1039/C8SC04228D
Cc1c(NC(c2nnc(-c3ccc(F)cc3)s2)C(C)O)ccc(C#N)c1Cl
Reaction #255603
DOI: 10.1039/C8SC04228D
COc1cccc(OC)c1CNC(=O)c1cc2cc(CC(C)NCC(O[Si](C)(C)C(C)(C)C)c3ccc(O)c(CO)c3)ccc2[nH]1
Reaction #274398
DOI: 10.1039/C8SC04228D
Cc1c(NC(c2nnc(-c3ccc(NC(=O)c4ccccc4)cc3)o2)C(C)O[Si](C)(C)C(C)(C)C)ccc(C#N)c1Cl
Reaction #278349
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC1CNCC(F)C1
Reaction #285476
DOI: 10.1039/C8SC04228D
CC(Cc1cccc(CC(=O)O)c1)NCC(O[Si](C)(C)C(C)(C)C)c1ccc(OCc2ccccc2)c2[nH]c(=O)ccc12
Reaction #302441
DOI: 10.1039/C8SC04228D
CC(C)(O[Si](C)(C)C(C)(C)C)[C@H]1COCc2nc3cnc4ccccc4c3n21
Reaction #308727
(11R)-11-(1-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinoline
収率 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)[C@H]1COCc2nc3cnc4ccccc4c3n21
Reaction #308728
2-[(11R)-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-11-yl]propan-2-ol
収率 91.6%DOI: 10.6084/m9.figshare.5104873.v1
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