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41022

N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3ccc(-c4ccc(Cl)s4)s3)C2=O)c1
Reaction #2865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1csc(-c2sccc2CCCCBr)c1
Reaction #172531
product
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172590
ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(NCCN2CCNC2=O)nc1-c1ccc(-c2cccs2)s1
Reaction #199185
DOI: 10.1039/C8SC04228D
Cc1ccccc1S(=O)(=O)Nc1cc(-c2cc3ccccc3s2)sc1C(=O)O
Reaction #222745
DOI: 10.1039/C8SC04228D
CCC1(CC)c2ccsc2-c2sccc21
Reaction #222904
DOI: 10.1039/C8SC04228D
Cl
Reaction #223018
DOI: 10.1039/C8SC04228D
BrC(Br)=Cc1ccc(-c2cccs2)s1
Reaction #224366
DOI: 10.1039/C8SC04228D
COC(OC)C(O)C=Cc1ccc(-c2cccs2)s1
Reaction #240505
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCCCCCCc1ccc(-c2cccs2)s1
Reaction #247725
DOI: 10.1039/C8SC04228D
CCc1ccc(-c2ccc(S(=O)(=O)Nc3onc(C)c3Br)s2)s1
Reaction #256534
DOI: 10.1039/C8SC04228D
CCCCCCCCC1(CCCCCCCC)c2ccsc2-c2sccc21
Reaction #259845
DOI: 10.1039/C8SC04228D
CCC1(COCCCCCCc2ccc(-c3ccc(B4OC(C)(C)C(C)(C)O4)s3)s2)COC1
Reaction #267602
DOI: 10.1039/C8SC04228D
Brc1ccc(-c2cccs2)s1
Reaction #274262
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc(-c2cccs2)s1
Reaction #275289
DOI: 10.1039/C8SC04228D
N#Cc1cccc(CN2CCC(NS(=O)(=O)c3ccc(-c4ccc(Cl)s4)s3)C2=O)c1
Reaction #276369
DOI: 10.1039/C8SC04228D
O=c1[nH]c2ccccc2n1CCNc1nccc(-c2ccc(-c3cccs3)s2)n1
Reaction #286174
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccc(S(=O)(=O)n3cccc3)s2)s1
Reaction #291686
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccc(C(=O)O)s2)s1
Reaction #296930
DOI: 10.1039/C8SC04228D
O=Cc1cc(-c2ccc(-c3cccs3)s2)sc1CO
Reaction #297459
DOI: 10.1039/C8SC04228D
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