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ClCCCCI

CC(C)COc1ccc(CN2C(=O)OC3(CCN(CCCN4CCOCC4)CC3)C2Cc2ccc(F)cc2)cc1.Cl.Cl
Reaction #40646
desired compound
Ausbeute 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
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(SCc2ccc(OC)cc2)CCCCC1
Reaction #50796
1-(carboethoxy)-1-(4-methoxybenzylthio)cyclohexane
Ausbeute 56.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOCCOCCCCCCCl)OCc1c2ccccc2cc2ccccc12
Reaction #59237
product
Ausbeute 41.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOCCOCCCCCl)OCc1c2ccccc2cc2ccccc12
Reaction #59238
product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOCCOCCCCCCCl)OCc1c2ccccc2cc2ccccc12
Reaction #61378
product
Ausbeute 41.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCOCCOCCCCCl)OCc1c2ccccc2cc2ccccc12
Reaction #61379
product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1C)N(CCCCl)c1ccccc1S2
Reaction #76463
title compound
Ausbeute 57.2%DOI: 10.6084/m9.figshare.5104873.v1
ClCCCN(CCc1cccnc1)Cc1ccncc1
Reaction #156179
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
O=C(O)C(CCCCCl)c1ccc(Cl)nc1
Reaction #191023
DOI: 10.1039/C8SC04228D
O=C(O)C(CCCCCl)c1ccc(OC(F)F)cc1
Reaction #196942
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
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