Substructure Search

1410569

CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)Cc3ccc(Cl)cc3)CC2)cc1.O=C([O-])C(O)C(O)C(=O)[O-]
Reaction #1759
trans-O-(4-Chlorophenylacetyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol tartrate
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cccnc1C=O
Reaction #7241
3-n-propoxypyridine-2-carboxaldehyde
Yield 113.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2nn3c(c2-c2ccnc4cc(CCC(=O)N(C)C)ccc24)CCC3)n1
Reaction #8366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COc2ccc3c(-c4c(-c5ccccn5)nn5c4CCC5)ccnc3c2)C1
Reaction #8372
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nc(CO)co1
Reaction #9002
(4-hydroxymethyl-oxazol-2-ylmethyl)-carbamic acid tert-butyl ester
Yield 28.4%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(-c2nc3ccccc3s2)cc1
Reaction #9069
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9075
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(CCCO)nc3N21
Reaction #12016
compound
Yield 50.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCN(C)CC4)s3)[nH]n2)cc(OC)c1
Reaction #45088
title compound
Yield 33.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3ccc(N4CCN(C)CC4)s3)[nH]n2)cc(OC)c1
Reaction #45089
title compound
Yield 32127.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3ccc(N4CCNC(C)(C)C4)s3)[nH]n2)cc(OC)c1
Reaction #45120
title compound
Yield 15.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3ccc(N4C[C@@H](C)N[C@@H](C)C4)s3)[nH]n2)cc(OC)c1
Reaction #45128
title compound
Yield 32.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](O)OCC1[C@@H](OCc1ccccc1)[C@H](Cc1cc(F)cc(F)c1)N(Cc1ccccc1)Cc1ccccc1
Reaction #48688
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](O[Si](CC)(CC)CC)[C@@H](C)[C@H](O)[C@H](C)C=O
Reaction #50360
31
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1cccc2oc(CO)c(C)c12
Reaction #57748
[4-(3-methoxypropyl)-3-methyl-1-benzofuran-2-yl]methanol
Yield 96.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)N[C@H]3CCCN(C(=O)OC(C)(C)C)C3)c(NC(N)=O)s2)cc1
Reaction #58613
light yellow solid
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)N[C@H]3CCCCN(C(=O)OC(C)(C)C)C3)c(NC(N)=O)s2)cc1
Reaction #58616
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1nnc2c(Br)cccc2c1N
Reaction #59368
title compound
Yield 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)c1nnc2c(Br)cccc2c1N
Reaction #59370
title compound
Yield 26.1%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCOc2ccccc21
Reaction #60347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next