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FC(F)(F)Cn1cc(-c2ccncc2)c(-c2ccc(OCc3ccccc3)cc2)n1
Reaction #62169
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(C(c2ccccc2)(c2ccccc2)n2nc(-c3ccc4ccccc4c3)c3ncccc32)cc1
Reaction #62339
title compound
Ausbeute 28.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(I)nn(C(c3ccccc3)(c3ccccc3)c3ccccc3)c2cn1
Reaction #62345
title compound
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc2c(I)nn(C(c3ccccc3)(c3ccccc3)c3ccccc3)c2cn1
Reaction #62386
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc2c(cc1Br)c(I)nn2C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #62408
title compound
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(/C=C/c2nn(C(c3ccccc3)(c3ccccc3)c3ccccc3)c3cc(F)c(Br)cc23)cc1
Reaction #62409
title compound
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(I)cc1)NC(C)=O
Reaction #66047
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(C)c(I)c1
Reaction #66504
3-iodo-N,4-dimethylbenzamide
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCNC(=O)c1ccccc1I
Reaction #77489
2-iodo-benzoic acid allylamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)Nc2ccc(-c3cccc([N+](=O)[O-])c3)cc21
Reaction #78950
4,4-Dimethyl-6-(3-nitrophenyl)-1,4-dihydrobenzo[d][1,3]oxazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncccc1-c1nc(C(F)(F)F)cn1-c1ccc(S(=O)(=O)CC[Si](C)(C)C)cc1
Reaction #80646
2-methyl-3-[1-[4-[[2-(trimethylsilyl) ethyl]sulfonyl]phenyl]-4-(trifluoromethyl) -1H-imidazol-2-yl]pyridine
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)cc(I)c2[nH]c1=O
Reaction #82624
5-iodo-7-chloro-1,4-dihydro-2,3-quinoxalinedione
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H]1O[C@H](CI)C[C@H]1O)(c1ccccc1)c1ccccc1
Reaction #83089
desired product
Ausbeute 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H]1O[C@H](CN=[N+]=[N-])C[C@H]1O)(c1ccccc1)c1ccccc1
Reaction #83090
desired product
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(I)c(C(=O)N2CCC[C@@H](C)[C@H]2CN2C(=O)c3ccccc3C2=O)c1
Reaction #89338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CN2C(=O)c3ccccc3C2=O)c1
Reaction #89339
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN(C(=O)c2cc(Cl)ccc2I)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89410
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN(C(=O)c2cc(Cl)ccc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89411
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN(C(=O)c2cc(F)ccc2I)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89453
title compound
Ausbeute 62.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN(C(=O)c2cc(F)ccc2-c2ncccn2)[C@@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89454
title compound
Ausbeute 56.9%DOI: 10.6084/m9.figshare.5104873.v1
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