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Cc1c[nH]cn1

CS(=O)(=O)NCCSc1cccc2nc(CC(=O)O)cn12
Reaction #5538
desired product
Ausbeute 51.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1NCCn2cc(-c3ccccc3OC)nc21
Reaction #6863
desired product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1cc(-c2ccc([N+](=O)[O-])cc2)nc1C=O
Reaction #7197
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C2SCC(=NO)CS2)ncn1Cc1ccccc1
Reaction #55456
crude product
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c([C@H]2SC[C@H](N)CS2)ncn1Cc1ccccc1
Reaction #55457
Trans 2-(1-benzyl-5-methyl-4-imidazolyl)-5-amino-1,3-dithiane
DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]cnc1CSCCNc1nnc(Cc2cccnc2)c(=O)[nH]1
Reaction #55497
title compound
Ausbeute 70.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(-c2ncc(-c3cnc(-c4cccnc4)[nH]3)cn2)c1
Reaction #70560
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CC[C@H](c3cccc(C(=O)O)c3)CC2)nc1Cl
Reaction #72107
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CC[C@@H](c3cccc(C(=O)O)c3)CC2)nc1Cl
Reaction #72109
title compound
Ausbeute 49.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)NC2CC=C(c3cccc(C(=O)O)c3)CC2)nc1Cl
Reaction #72112
title compound
Ausbeute 20.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(CC(N=O)C(C)(C)Cl)c([N+](=O)[O-])n1
Reaction #75443
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)C(C)(C)NCCCNC(C)(C)C(Cn1cc(C)nc1[N+](=O)[O-])=NO
Reaction #75444
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc([N+](=O)[O-])n1CC(N=O)C(C)(C)Cl
Reaction #75445
3-Chloro-3-methyl-2-nitroso-1-(5-methyl-2-nitro-1H-imidazol-1-yl)butane
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(COCCC(F)(F)F)cc(C(C)=O)n2)ccc1-n1cnc(C)c1
Reaction #87368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(COCC(F)(F)F)cc(CC(N)=O)n2)ccc1-n1cnc(C)c1
Reaction #87407
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(CC#N)cc(COCC(F)(F)F)n2)ccc1-n1cnc(C)c1
Reaction #87412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(COCC3CC3)cc(COCC(F)(F)F)n2)ccc1-n1cnc(C)c1
Reaction #87424
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(COCC(F)(F)F)cc(CN(C)C)n2)ccc1-n1cnc(C)c1
Reaction #87447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2nc(COCC(F)(F)F)cc(OCC3CC3)n2)ccc1-n1cnc(C)c1
Reaction #87457
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCCc1cncn1Cc1ccc(C#N)cc1[N+](=O)[O-]
Reaction #164063
methanesulfonic acid 2-[3-(4-cyano-2-nitrobenzyl)-3H-imidazol-4-yl]ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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