Поиск подструктуры

c1cc(N2CCCC2)ccn1

CCC[C@H](N)C(=O)NC1CCN(c2ccn3c(=O)c(C(=O)O)ccc3c2)C1
Reaction #1942
amino acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1946
amino acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC[C@@H]([C@H](C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1972
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CC[C@H]([C@@H](C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1973
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)cn2c(=O)c(C(=O)O)c(N3CCC(C(C)N)C3)c(C3CC3)c12.Cl
Reaction #1974
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N2CCC(C(C)(C)N)C2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12.Cl
Reaction #1977
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(N)C1CCN(c2c(F)cn3c(=O)c(C(=O)O)cc(C4CC4)c3c2C)C1.Cl
Reaction #1978
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCOc1ccc(-c2nc3cc(C(=O)OCCCCCCCC)ccc3o2)cc1
Reaction #5377
2-(4-decyloxyphenyl)-5-octyloxycarbonyl benzooxazole
Выход 49.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #5640
product
Выход 649.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1cccc(C=O)c1)(c1ccccc1)c1ccccc1
Reaction #50880
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cc(C(C)(C)C)n[nH]3)c2)CN1C(=O)OC(C)(C)C
Reaction #73366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCCCBr)OCc1ccccc1
Reaction #77178
Benzyl-8-bromoctanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N3C(=O)c4ccccc4C3=O)nc3ccccc3c2n1CC(C)(C)OC(=O)CN1C(=O)c2ccccc2C1=O
Reaction #91971
product
Выход 85.8%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CCN(c2ccnc(Cl)c2)C1
Reaction #164482
title compound
Выход 30.6%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CCN(c2ccnc(Cl)c2)C1
Reaction #164483
desired product
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2c1CN(C(=O)CC(=O)C1CC1)CC2
Reaction #168008
1-(2-chloro-4-methyl-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)-3-cyclopropylpropane-1,3-dione
Выход 52.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cccc(Nc2nccc(Sc3ccccc3)n2)c1
Reaction #168899
desired product
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCCC2)c2ccc(OCc3ccc(C#N)cc3)cc2n1
Reaction #178113
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)Nc2cccc(C(C)Nc3cncc(Cl)n3)c2)cn1
Reaction #179117
DOI: 10.1039/C8SC04228D
Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #182966
DOI: 10.1039/C8SC04228D
Страница 1Далее