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II

CCc1nc(-c2ccccc2)[nH]c(=O)c1I
Reaction #1544
6-ethyl-5-iodo-2-phenyl-4(3H)-pyrimidinone
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2CCC1I
Reaction #1830
product
Ausbeute 57.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([CH2][Mg][Br])cc1
Reaction #1846
Anisylmagnesium Bromide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CO)cc1I
Reaction #3068
3-iodo-4-methylbenzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc3cc4c(cc3c2sn1CCc1ccccn1)OCO4
Reaction #3367
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCn1sc2nc(-c3ccccc3)ncc2c1=O
Reaction #3368
title compound
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(-c3ccccc3)nc2sn1Cc1ccccc1
Reaction #3369
title compound
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(-c3ccccc3)nc2sn1CCN1CCOCC1
Reaction #3370
title compound
Ausbeute 60.8%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(-c3ccccc3)nc2sn1CCc1ccccc1
Reaction #3371
title compound
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(-c3ccccc3)nc2sn1Cc1ccccn1
Reaction #3372
title compound
Ausbeute 81.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(-c3ccccc3)nc2sn1CCc1ccccn1
Reaction #3373
title compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(N3CCCCC3)nc2sn1CCc1ccccn1
Reaction #3374
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]sc2nc(N3CCCCC3)ncc12
Reaction #3375
title compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cnc(N3CCOCC3)nc2sn1CCN1CCCCC1
Reaction #3376
title compound
Ausbeute 50.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ncc2c(=O)n(CCc3ccccn3)sc2n1
Reaction #3377
title compound
Ausbeute 56.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ncc2c(=O)n(CCN3CCCCC3)sc2n1
Reaction #3378
title compound
Ausbeute 85.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(I)c(CC(=O)O)c1
Reaction #4376
2-iodo-5-methoxybenzeneacetic acid
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(I)c(CCC(C)=O)c1
Reaction #4377
1-(2-iodo-5-methoxyphenyl)butane-3-one
Ausbeute 82.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(SCC#N)c2c1
Reaction #4408
5-methoxy-3-cyanomethylthioindole
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(=O)n([C@H]2CC[C@@H](CO)O2)cc1I
Reaction #4982
iodide
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
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