Recherche de Sous-structure

763912

CC(C)COc1ccc(CN2C(=O)OC3(CCN(CCCN4CCOCC4)CC3)C2Cc2ccc(F)cc2)cc1.Cl.Cl
Reaction #40646
desired compound
Rendement 59.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cc(OCCCCl)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49603
4-chloro-5-(3-chloropropoxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Rendement 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CNC1=NC=NC2C1C(I)=CN2C(C)C
Reaction #61689
desired product
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1C)N(CCCCl)c1ccccc1S2
Reaction #76463
title compound
Rendement 57.2%DOI: 10.6084/m9.figshare.5104873.v1
ClCCCN(CCc1cccnc1)Cc1ccncc1
Reaction #156179
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC(CCl)CI
Reaction #158285
title compound
Rendement 74.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CC(O[Si](C)(C)C(C)(C)C)CC3c2ccc(F)c(F)c2)ccc1-c1cnc(C)o1
Reaction #158288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(C#N)(CCCCl)CC1
Reaction #177904
DOI: 10.1039/C8SC04228D
COc1ccc(CN2C(=O)C(CCCCl)Cc3cc([N+](=O)[O-])ccc32)cc1
Reaction #179031
DOI: 10.1039/C8SC04228D
O=C1c2c(-c3cccc(F)c3)noc2CCC1CCCCl
Reaction #180603
DOI: 10.1039/C8SC04228D
O=C1COc2ccccc2N1CCCCl
Reaction #183054
DOI: 10.1039/C8SC04228D
O=c1oc2cc(F)ccc2n1CCCCl
Reaction #184868
DOI: 10.1039/C8SC04228D
O=C(O)c1cc(S(=O)(=O)CCCCl)ccc1O
Reaction #188656
DOI: 10.1039/C8SC04228D
FC(F)(Cl)C(F)(Cl)C(F)(F)C(F)(F)I
Reaction #196440
DOI: 10.1039/C8SC04228D
Cc1c(CCCCl)sc2ccc(F)cc12
Reaction #197597
DOI: 10.1039/C8SC04228D
ClCCCOc1cccnc1
Reaction #199915
DOI: 10.1039/C8SC04228D
O=C1COc2c(F)cc(Br)cc2N1CCCCl
Reaction #200206
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)NCCCCl
Reaction #204328
DOI: 10.1039/C8SC04228D
COC(=O)C(CCCCl)c1ccccc1
Reaction #206378
DOI: 10.1039/C8SC04228D
CC(C)Oc1cncc(OCCCCl)c1
Reaction #208066
DOI: 10.1039/C8SC04228D
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