Busqueda de Subestructura

786639

COC(=O)c1ccc2c(c1)/C(=C/Cn1ccc3cccnc31)c1ccccc1CO2
Reaction #5134
Methyl (E)-11-[2-(7-aza-1-indolyl)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(Cl)nc3N21
Reaction #12005
desired compound
Rendimiento 65.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(Br)nc3N21
Reaction #12009
(4R,9aR)-6-Bromo-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@@H]2Cc3ccc(Br)nc3N21
Reaction #12010
(4R,9aS)-6-Bromo-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cc3n(c2n1)[C@H](C)CN(C(=O)OC(C)(C)C)C3
Reaction #12011
desired product
Rendimiento 71.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)CC2Cc3cccnc3N21
Reaction #12025
(R)-4-Methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)O)Cc2c(C=O)c3ccc(Cl)nc3n21
Reaction #12028
desired compound
Rendimiento 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cc4cccnc4[nH]3)c2c1
Reaction #53693
2-methylsulfonyl-N-[3-(1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Rendimiento 45.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(-c3nc4ccc(F)nc4o3)cnc21
Reaction #69003
5-fluoro-2-(1-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-oxazolo[5,4-b]pyridine
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2cn(C(=O)c3c(Cl)cccc3Cl)c3ncc(B4OC(C)(C)C(C)(C)O4)cc23)c1F
Reaction #88382
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4cnn(-c5ncccn5)c4)cc23)c1F
Reaction #88383
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCCN(c2ccnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88540
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)OC(C)(C)C)[C@H]1CCCN(c2ccnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88541
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2cnc(C#N)cc2c2c(N3CC[C@H](O)C3)c(Cl)cnc21
Reaction #88549
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cn1)[nH]c1ncc(Cl)c(N3CC[C@H](O)C3)c12
Reaction #88550
title compound
Rendimiento 63.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2ccnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88551
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)OC(C)(C)C)[C@H]1CCN(c2ccnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88552
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2cnc(C#N)cc2c2c(N3CC[C@H](N)C3)ccnc21
Reaction #88588
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2cnc(C#N)cc2c2c(N3CC[C@H](NCC(F)(F)F)C3)ccnc21
Reaction #88589
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cn1)[nH]c1nccc(N3CC[C@H](NCC(F)(F)F)C3)c12
Reaction #88590
title compound
Rendimiento 5.0%DOI: 10.6084/m9.figshare.5104873.v1
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