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156013

COC(=O)[C@@H]1[C@@H]2C[C@@H](OC(C)=O)[C@@H]([C@H]2I)N1[C@H](C)c1ccccc1
Reaction #543956
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(I)c1C(=O)Nc1ccccc1S(C)=O
Reaction #919071
DOI: 10.1039/C8SC04228D
Cc1c(I)cc(Cl)cc1C(=O)O
Reaction #1137622
5-chloro-3-iodo-2-methylbenzoic acid
Ausbeute 158.9%DOI: 10.6084/m9.figshare.5104873.v1
Ic1c2ccccc2c(-c2ccccc2)c2ccccc12
Reaction #1726662
yellow solid
Ausbeute 117.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)c1c(I)c2cnc(Cl)nc2n1CCNC(=O)OC(C)(C)C
Reaction #1862482
tert-butyl N-[2-[2-chloro-6-(diethoxymethyl)-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl]ethyl]carbamate
Ausbeute 22.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(I)c1C(=O)NC(C)(C)CS(C)=O
Reaction #1915550
methyl 3-iodo-2-(1,1-dimethyl-2-methylsulfinylethylaminocarbonyl)-benzoate
Ausbeute 137.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(I)c1C(=O)Nc1ccccc1S(C)=O
Reaction #1915551
2-iodo-6-methyl-2′-methylsulfinylbenzanilide
Ausbeute 124.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1cccc(I)c1C(=O)NC(C)(C)CS(C)=O
Reaction #1915556
n-butyl 2-(1,1-dimethyl-2-methylsulfinylethylaminocarbonyl)-3-iodobenzoate
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cnc2c(-c3ccc(F)c(I)c3)cnnc21
Reaction #1933185
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2cnnc3c2ncn3C2CC2)cc1I
Reaction #1933239
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Ic1c2ccccc2c(-c2ccccc2)c2ccccc12
Reaction #2148499
yellow solid
Ausbeute 117.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(I)c1C(=O)NC(C)(C)CS(C)=O
Reaction #2248447
DOI: 10.1039/C8SC04228D
CCCCOC(=O)c1cccc(I)c1C(=O)NC(C)(C)CS(C)=O
Reaction #2397460
DOI: 10.1039/C8SC04228D
Ic1c2ccccc2c(-c2ccccc2)c2ccccc12
Reaction #2423550
DOI: 10.1039/C8SC04228D