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12605

CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1=C(OC)CCC1=O
Reaction #68746
2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone
Ausbeute 75.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1C(=O)CCC1=O
Reaction #68747
2-(4′-chloro-4-ethylbiphen-3-yl)-1,3-cyclopentanedione
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2CC(C(=O)O)Nc3cc(Cl)cc(Cl)c32)cc1
Reaction #75652
Compound 20
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2cccc(Br)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75670
Compound 38
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3scc(C)c3c2C=O)n1
Reaction #80271
desired compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3scc(C)c3c2C(=O)O)n1
Reaction #80272
desired compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1C(=O)CC(C)(C)c2ccc(C#C[Si](C)(C)C)cc21
Reaction #80728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CCC(CN2C(=O)c3ccccc3C2=O)N(C(=O)c2ccccc2-c2ccccc2)C1
Reaction #89090
2-((1-(biphenylcarbonyl)-5,5-dimethoxypiperidin-2-yl)methyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C(=O)Cl)c2ccccc21
Reaction #155388
10-Methylacridan-9-carboxylic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C(=O)Cl)c2ccccc21
Reaction #155390
acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
COCCCNC(=O)c1ccc(OCc2c(-c3ccccc3)noc2C)nc1
Reaction #170308
title compound
Ausbeute 82.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2CCC2)cn1
Reaction #170319
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2CCOCC2)cn1
Reaction #170322
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N(C)C2CCOCC2)cn1
Reaction #170339
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1cc(OCc2ccccc2)ccn1
Reaction #170344
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1cc(C(=O)NC2CCOCC2)ccn1
Reaction #170349
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N(C)C(C)C)cn1
Reaction #170359
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2cccc(Cl)c2)c1COc1ccc(C(=O)NC2CCOCC2)cn1
Reaction #170405
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccc(Cl)cc2)c1COc1ccc(C(=O)NC2CCOCC2)cn1
Reaction #170425
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
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