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279437

CCCCCOCC1CCC(CN(Cc2ccccc2)S(=O)(=O)NC(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #52014
title compound
Rendimiento 73.9%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@H](COCCCBr)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53846
trans-N-[4-(3-Bromo-propoxymethyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(CCO)CCO
Reaction #81529
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #159165
title compound
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC12CCC(N(C)C(=O)C(=O)N(C)C)(CC1)c1nc(C(=O)NCc3ccc(F)c(C)c3)c(O)c(=O)n1C2
Reaction #162913
title compound
Rendimiento 3.8%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #167108
title compound
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(OC)C(CCCCC)C(=O)OC(C)(C)C
Reaction #186713
DOI: 10.1039/C8SC04228D
NS(=O)(=O)Oc1ccc(-c2ccccc2[N+](=O)[O-])cc1
Reaction #193461
DOI: 10.1039/C8SC04228D
O=C1OCCC1SCCCOS(=O)(=O)C(F)(F)F
Reaction #204450
DOI: 10.1039/C8SC04228D
COc1cc(S(=O)(=O)N(C)C)c(OC)cc1NC(=O)C(C)(O)C(F)(F)F
Reaction #239026
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(CBr)cc(C(C)(C)C)n1
Reaction #240357
DOI: 10.1039/C8SC04228D
CCOC(=O)COCCc1cc(F)ccc1F
Reaction #241561
DOI: 10.1039/C8SC04228D
C=CCC(C(=O)OC(C)C)C(OCC)C(=O)OC(C)C
Reaction #254926
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(C(=O)O)cc(C(C)(C)C)n1
Reaction #267968
DOI: 10.1039/C8SC04228D
CCc1ccc2c(-c3cccc(Cl)c3)c(CCCCCOC)c(-c3ccccc3)nn12
Reaction #271335
DOI: 10.1039/C8SC04228D
CCOC(=O)COCCc1cccc(OC(F)(F)F)c1
Reaction #284235
DOI: 10.1039/C8SC04228D
COc1cc(S(=O)(=O)Nc2ccccc2)c(OC)cc1NC(=O)C(C)(O)C(F)(F)F
Reaction #290933
DOI: 10.1039/C8SC04228D
CC(O[Si](C)(C)C)(C(=O)Nc1ccc(I)c([N+](=O)[O-])c1Cl)C(F)(F)F
Reaction #291389
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NS(=O)(=O)OC[C@@H]1C[C@@H](n2ccc3c(N[C@@H]4CCc5ccccc54)ncnc32)C[C@@H]1O
Reaction #309342
title compound
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1ccccc1N1CCN(C(=O)[C@@H](Cc2ccc(Cl)cc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)OCC2c3ccccc3-c3ccccc32)CC1
Reaction #315262
desired compound
Rendimiento 86.3%DOI: 10.6084/m9.figshare.5104873.v1
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