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CC(C)(N)c1ccccc1

COc1cccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49353
4-methoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1cccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49362
4-methoxymethoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 96.2%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(I)c2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49363
4-methoxymethoxy-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(OC)ccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49547
4-methoxymethoxy-5-methoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(OC)cc(I)c2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49548
4-methoxymethoxy-5-methoxy-3-hydroxy-7-iodo-2-(1-methyl-1-phenyl ethyl)isoindolinone
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(C)ccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49553
4-methoxymethoxy-5-methyl-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(C)cc(I)c2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49554
4-methoxymethoxy-5-methyl-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)NC2(c3ccccc3)CC2)cc1-c1cc(F)n2nc(-c3ccc(F)cc3)c(C(=O)N(C)C(=O)OC(C)(C)C)c2c1
Reaction #72328
tert-butyl 7-fluoro-2-(4-fluorophenyl)-5-(2-methyl-5-(1-phenylcyclopropylcarbamoyl)phenyl)pyrazolo[1,5-a]pyridine-3-carbonyl(methyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(F)c2)CCCN1c1ccn2ncc(NC(=O)N3CC(O)C3)c2n1
Reaction #92272
final product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(Br)c2)COCC(N)=N1
Reaction #168698
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=NC(C)(c2cccc(N=[N+]=[N-])c2)COC1
Reaction #168699
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=NC(C)(c2cccc(N)c2)COC1
Reaction #168700
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=NC(c2cccc(Br)c2)C(CF)OC1
Reaction #168710
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=NC(CF)(c2cccc(N=[N+]=[N-])c2)COC1
Reaction #168711
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=NC(CF)(c2cccc(NC(=O)c3ccc(Br)cn3)c2)COC1
Reaction #168712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=N[C@](CF)(c2cccc(N)c2)COC1
Reaction #168714
(R)-[5-(3-Amino-phenyl)-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC(c2ccnc(C(F)(F)F)c2)(c2ccc(O)c(-c3cnccn3)c2)c2cccc(F)c21
Reaction #176027
DOI: 10.1039/C8SC04228D
CCn1cc(C2=NC(c3ccc(F)cc3)(c3ccnc(F)c3)C(C)N2)ccc1=O
Reaction #183679
DOI: 10.1039/C8SC04228D
CC1(c2cc(Br)ccc2F)COCC(N)=N1
Reaction #187846
DOI: 10.1039/C8SC04228D
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)NC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #192309
DOI: 10.1039/C8SC04228D
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