Substructure Search

8756

CNC(=S)C1(c2cnc3ccccc3c2)CCCCC1=O
Reaction #6005
(±)-N-methyl-2-oxo-1-(quinolin-3-yl)cyclohexanecarbothioamide
Yield 9.4%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H]1CCCN1N=C1CCCCC1c1cccnc1
Reaction #6007
[2S]-2-(methoxymethyl)-1-[2-(pyrid-3-yl)cyclohexylidenamino]pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1(c2cncc(Br)c2)CCCCC1=O
Reaction #224166
DOI: 10.1039/C8SC04228D
CNC(=S)C1(c2ccc(Cl)nc2)CCCCC1=O
Reaction #246747
DOI: 10.1039/C8SC04228D
CCC12CC(C)(O)C(O)(c3cccnc3)CC1CCc1cc(O)ccc12
Reaction #250745
DOI: 10.1039/C8SC04228D
CNC(=S)C1(c2cccnc2)CCCCC1=CC#N
Reaction #285108
DOI: 10.1039/C8SC04228D
CNC(=S)C1(c2cccnc2)CCCCC1=Nc1ccccc1
Reaction #380577
DOI: 10.1039/C8SC04228D
COCC1CCCN1N=C1CCCCC1c1cnc2ccccc2c1
Reaction #402957
DOI: 10.1039/C8SC04228D
CC1(c2cccnc2)C(=C=S)C(=C=S)CCC1=CC#N
Reaction #758745
DOI: 10.1039/C8SC04228D
CC[C@@]12C[C@@](C)(O)[C@](O)(c3cccnc3)C[C@H]1CCc1cc(O)ccc12
Reaction #809616
title compound
Yield 6.3%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CCCN1N=C1CCCCC1c1cccnc1
Reaction #904637
DOI: 10.1039/C8SC04228D
CNC(=S)C1(c2cccnc2)CCCCC1=CC#N
Reaction #1117424
(±)-2 -cyanomethylene-N-methyl-1-(pyrid-3 -yl)cyclohexane carbothioamide
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccnc2)C(=C=S)C(=C=S)CCC1=CC#N
Reaction #1117433
2-(pyrid-3-yl)-2-methyldithiocarbonyl-1-cyanomethylenecyclohexane
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2C(=O)C(C(=O)OC)(C1)c1ccc(OC)nc1C2CC
Reaction #1165443
10-Ethyl-7,8,9,10-tetrahydro-2-methoxy-7-methylene-11-oxo-5,9-methanocycloocta[b]pyridine-5(6H)-carboxylic Acid Methyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN(C(=O)OC(C)(C)C)C1(c2cccnc2)CCCCC1=O
Reaction #1284666
2-(N,N'-di-t-butoxycarbonylhydrazino)-2-(pyrid-3-yl)cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1(c2cccnc2)CCCCC1=Nc1ccccc1
Reaction #1284670
N-methyl-2-phenylimino-1-(3-pyridyl)cyclohexanecarbothioamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1(c2ccc3nc(C)cn3c2)CCCCC1=O
Reaction #1527428
title compound
Yield 78.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1(c2ccc3nc(C)cn3c2)CCCCC1=O.O=C(O)[C@](O)(C(=O)c1ccccc1)[C@](O)(C(=O)O)C(=O)c1ccccc1
Reaction #1527429
(+)-N-methyl-1-(2-methylimidazo[1,2-a]pyridin-6-yl)-2-oxocyclohexanecarbothioamide (+)-dibenzoyl-D-tartrate
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1(c2ccc3nc(C)cn3c2)CCCCC1O
Reaction #1539109
title compound
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1(c2ccc3nc(C(F)(F)F)cn3c2)CCCCC1O
Reaction #1539110
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
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