部分構造検索

C1CC(OC1)CN

O=C1CCC(C(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2Cl)O1
Reaction #1871
2',5-dichloro-2-(5-oxotetrahydrofuran-2-carbonyl) aminobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@@H]2O[C@@]3(CO)CO[C@@H]2[C@H]3O)c(=O)[nH]c1=O
Reaction #6877
nucleoside
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@]23CO[C@@H]([C@H](n4cc(C)c(=O)[nH]c4=O)O2)[C@H]3O)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6878
nucleoside
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CC3CCC(C2)O3)cc1
Reaction #8676
benzylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)N1CC2CCC(C1)O2
Reaction #8677
Diethyl 2-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)malonate
DOI: 10.6084/m9.figshare.5104873.v1
Oc1nc(-c2nn(Cc3ccccc3F)c3ncccc23)nc(O)c1N1CC2CCC(C1)O2
Reaction #8678
2-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-5-(8-oxa-3-azabicyclo-[3.2.1]oct-3-yl)-4,6-pyrimidinediol
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1ccc(NCC2CCCO2)c(Cl)c1
Reaction #54620
2-chloro-4-amino-N-tetrahydrofurfurylaniline monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C[C@H]1C[C@H](S)CO1)OCc1ccccc1
Reaction #83058
desired product
収率 60.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(-c3nc4ccccc4o3)ccc2n1CC1CCCO1
Reaction #161460
title compound
収率 127.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\scc(C(C)(C)C)n1C[C@H]1CCCO1
Reaction #165709
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cn(C2CC(O)C(CN)O2)c(=O)[nH]c1=O
Reaction #188950
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)NC1Cc2c(n(CC3OCCC3O)c3ccc(C#N)cc23)C1
Reaction #190599
DOI: 10.1039/C8SC04228D
CC1CC(C)CN(CC2CCC(C)(C(C)(C)COc3ccc(Cl)cc3)O2)C1
Reaction #191383
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1OC(n2cnc3c(O)ncnc32)C(O)C1O
Reaction #194239
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC1CC(n2ccc(=O)[nH]c2=O)OC1(CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)C(NCc1ccccc1)NCc1ccccc1
Reaction #207811
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1OC(n2ccc(=O)[nH]c2=O)C(O)C1O
Reaction #213402
DOI: 10.1039/C8SC04228D
Cc1cn([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CN=[N+]=[N-])O2)c(=O)[nH]c1=O
Reaction #217137
5'-azido-3'-O-t-butyldimethylsilyl-5'-deoxythymidine
収率 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(C(=O)NC(Cc2ccccc2)C(O)CC(C)C(=O)NCCC2=CCCCC2)cc(N2CCCC2=O)c1
Reaction #227734
DOI: 10.1039/C8SC04228D
CC1CC(C(CC2CCCCC2)NC(=O)C(Cc2cscn2)NC(=O)OC(C)(C)C)OC1=O
Reaction #232256
DOI: 10.1039/C8SC04228D
O=CN(O)C(CS(=O)(=O)N1CCc2ccc(Cl)cc2C1)C1CCCO1
Reaction #246725
DOI: 10.1039/C8SC04228D
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