부분 구조 검색

12704

Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccncc3)c2c1
Reaction #7348
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-pyridinyl)quinolin-6-ol
수율 20.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc3ccccc3o2)ccc1Cc1ccncc1
Reaction #7848
2-[3-methoxy-4-(pyridin-4-ylmethyl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)cc(F)n1
Reaction #8400
4-bromo-2,6-difluoropyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn(CCCCCl)c(=O)n(C(=O)c3ccccc3)c2=O)ccn1
Reaction #40955
title compound
수율 25.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccncc2F)c(OC)n1
Reaction #40973
title compound
수율 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccncc1
Reaction #41048
title compound
수율 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([N+](=O)[O-])cc1-c1ccncc1Cl
Reaction #41775
3-chloro-4-(2-methyl-5-nitrophenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(Oc2ccncc2)cc1)NC(=O)OC(C)(C)C
Reaction #41907
(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester
수율 20.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(-c2ccncc2)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45350
Methyl{[5 ′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}[3-pyridin-4-yl-5-(trifluoromethyl)benzyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(-c2csc3c(-c4ccncc4)cnc(N)c23)cc1
Reaction #45409
desired product
수율 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccnc(Cl)c2)CC1
Reaction #48128
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCOCC4)n(-c4ccnc(Cl)c4)c3cc2Br)CC1
Reaction #48165
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCC(F)(F)CC4)n(-c4ccnc(Cl)c4)c3cc2Br)CC1
Reaction #48167
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccncc3)c2c1
Reaction #53692
2-methylsulfonyl-N-(3-pyridin-4-yl-1H-indazol-5-yl)benzenesulfonamide
수율 15.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC3CCCO3)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57147
title compound
수율 11.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1ccc(-c2nn(CC(F)(F)F)cc2-c2ccnc3[nH]ccc23)cc1
Reaction #57148
title compound
수율 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ccc3c(-c4sc(C)nc4-c4ccc([N+](=O)[O-])cc4)ccnc32)cc1
Reaction #57218
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ccc3c(-c4oc(C)nc4-c4ccc([N+](=O)[O-])cc4)ccnc32)cc1
Reaction #57221
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3c2cc(C=O)n3S(=O)(=O)c2ccccc2)c(-c2ccc(NC(=O)Nc3ccccc3)cc2)n1
Reaction #57231
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc(-c2cc3c(-c4cn(C)nc4-c4ccc([N+](=O)[O-])cc4)ccnc3[nH]2)cc1
Reaction #57252
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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