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294320

CC(C)CCc1ccccc1N1CCN(C(=O)OC(C)(C)C)CC1=O
Reaction #179811
DOI: 10.1039/C8SC04228D
Cn1cc(-c2cc(S(C)(=O)=O)ccc2CCC2CC2)ccc1=O
Reaction #605693
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(S(C)(=O)=O)ccc2CCC2CC2)c2ccccc2c1=O
Reaction #605695
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(S(C)(=O)=O)ccc2CCC2CC2)ccc1=O
Reaction #662963
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(S(C)(=O)=O)ccc2CCC2CC2)c2ccccc2c1=O
Reaction #662965
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCC(Oc2ccc3c(c2I)CCC(C2(C)COC(=O)N2)C3)CC1
Reaction #752221
DOI: 10.1039/C8SC04228D
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3c(c2I)CC[C@H]([C@]2(C)COC(=O)N2)C3)CC1
Reaction #797072
(R)-4-((S)-6-(trans-4-tert-butylcyclohexyloxy)-5-iodo-1,2,3,4-tetrahydronaphthalen-2-yl)-4-methyloxazolidin-2-one
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(C)(C)C2(OC2c2cc(Br)ccc2I)C1=O
Reaction #966243
2-(5-bromo-2-iodophenyl)-4,4,6,6-tetramethyl-1,5-dioxaspiro[2.4]heptan-7-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)N1CCc2cc(-c3ccccc3)c3c(c2CC1)C(C)(C)CC3
Reaction #1012402
sub-title compound
Ausbeute 46.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2cccc(Cl)c2)C2(C(=O)Nc3cc(Cl)ccc32)C(c2cc(Cl)ccc2-n2ccnc2)N1
Reaction #1182298
6-chloro-2′-(5-chloro-2-imidazol-1-yl-phenyl)-4′-(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione
Ausbeute 5.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(C)(C)C2(OC2c2cc(Br)ccc2I)C1=O
Reaction #1280403
2-(5-bromo-2-iodophenyl)-4,4,6,6-tetramethyl-1,5-dioxaspiro[2.4]heptan-7-one
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C1CCC(C2CCC(CCC)CC2)CC1)C(O)c1c(F)cc(C)cc1I
Reaction #1331370
1-(2-Fluoro-6-iodo-4-methyl-phenyl)-2-(4′-propylbicyclohexyl-4-yl)-prop-2-en-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CCC(C2CCC(C3Cc4cc(C)cc(F)c4C3=O)CC2)CC1
Reaction #1331371
7-Fluoro-5-methyl-2-(4′-propylbicyclohexyl-4-yl)-indan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1ccccc1I
Reaction #1523698
desired compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1ccccc1I
Reaction #1523701
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1ccccc1N1CCN(C(=O)OC(C)(C)C)CC1=O
Reaction #1523702
title compound
Ausbeute 29.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1CC[C@H](Oc2ccc3c(c2I)CC[C@H]([C@]2(C)COC(=O)N2)C3)CC1
Reaction #1889288
(R)-4-((S)-6-(trans-4-tert-butylcyclohexyloxy)-5-iodo-1,2,3,4-tetrahydronaphthalen-2-yl)-4-methyloxazolidin-2-one
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1ccccc1I
Reaction #2242939
DOI: 10.1039/C8SC04228D