Substructure Search

6457

CC(N)COc1ccc(C#N)cc1
Reaction #1019
desired product
Yield 27.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)ccc1OCC(C)N
Reaction #1020
desired product
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1021
desired product
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Reaction #1271
Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(CCl)c1ccsc1S(=O)(=O)NC(C)(C)C
Reaction #1536
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(S(=O)(=O)Nc2ccc3nsnc3c2)cc1
Reaction #1720
4-ethylamino-N-(2,1,3-benzothiadiazol-5-yl)-1-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(C(O)c2cc(Cl)ccc2NCC(C)(C)C)c(OC)c1
Reaction #1887
crystal
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2ccccc2)ccc1C(O)c1cc(Cl)ccc1NCC(C)(C)C
Reaction #1905
α-(4-benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
NC(C1CC1)C1CCN(Cc2ccccc2)C1
Reaction #1990
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(CC(CC)NCc1ccccc1)P(=O)(OCC)OCC
Reaction #2067
tetraethyl 3-benzylaminopentane-1,1-bisphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1NCCN1CCC(C(=O)c2ccc(F)cc2)CC1
Reaction #2557
title compound
Yield 66.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)c1
Reaction #2562
title compound
Yield 46.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2563
title compound
Yield 20.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NCc1ccccc1CC(C(=O)OCC[Si](C)(C)C)N1C(=O)c2ccccc2C1=O)C(=O)OC(C)(C)C
Reaction #2810
title compound
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)c1[nH]c2c(c1C)C[C@@H]1CN(Cc3ccco3)CC[C@@]1(c1cccc(OC)c1)C2.Cl
Reaction #2973
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(c2ccc3c(c2)OCO3)CNC1c1ccc(OC)cc1
Reaction #3104
title compound
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3137
hydrate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3140
hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(CCc1cc(OC)ccc1I)N(C)C.Cl
Reaction #4381
2-Iodo-5-methoxy-N,N-dimethylalphapentylbenzenepropanamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1CNc1cccnc1N
Reaction #4388
2-amino-3-(2-methylbenzylamino)pyridine
Yield 34.4%DOI: 10.6084/m9.figshare.5104873.v1
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