Recherche de Sous-structure

[BH4-].[Na+]

C1CCC(NCCNC2CCCCC2)CC1
Reaction #46971
N,N′-Dicyclohexylethylenediamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OCc2ccccc2)c2[nH]c(=O)sc12
Reaction #206588
DOI: 10.1039/C8SC04228D
CC(=O)Oc1cccc2sc(-c3ccc(C)cc3)nc12
Reaction #237251
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nc3c(OC(C)=O)cccc3s2)cc1
Reaction #263076
DOI: 10.1039/C8SC04228D
CC(=O)Oc1cccc2sc(-c3ccc(C(=O)O)cc3)nc12
Reaction #785312
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc(OCc2ccccc2)c2[nH]c(=O)sc12
Reaction #836422
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(OCc2ccccc2)c2[nH]c(=O)sc12
Reaction #836423
title compound
Rendement 93.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2c(OCc3ccccc3)ccc([C@@H](O)CBr)c2s1
Reaction #836424
title compound
Rendement 69.8%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2c(OCc3ccccc3)ccc([C@H](CBr)OC3CCCCO3)c2s1
Reaction #836425
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=CO.O=c1[nH]c2c(O)ccc([C@@H](O)CNCCCCCCOCCCCc3ccccc3)c2s1
Reaction #836426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)Cc1ccc(C(=O)Nc2nc3c(OCc4ccccc4)ccc(N4CCOCC4)c3s2)cc1
Reaction #1027402
DOI: 10.1039/C8SC04228D
CCOc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CS5)CC3)nc12
Reaction #1100106
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)nc12
Reaction #1100107
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)OCCO5)CC3)nc12
Reaction #1100108
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(N2CCCCC2)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #1147494
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(N2CCCCC2)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #1147495
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)Cc1ccc(C(=O)Nc2nc3c(OCc4ccccc4)ccc(N4CCOCC4)c3s2)cc1
Reaction #1150213
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(N2CCCCC2)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #1150232
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(N2CCCCC2)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #1150233
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc2c(O)ccc(N3CCOCC3)c2s1)c1ccc(CCl)cc1
Reaction #1150271
title compound
Rendement 18.0%DOI: 10.6084/m9.figshare.5104873.v1
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