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1329393

CN(CCCC(=O)c1ccc(F)cc1)CC1CCN(Cc2ccccc2)CC1
Reaction #204148
DOI: 10.1039/C8SC04228D
O=C1COC2(CCN(CCCC(=O)c3ccc(F)cc3)CC2)CN1
Reaction #310549
9-[3-(4-fluorobenzoyl)propyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCI)c1ccc(F)cc1O
Reaction #398962
DOI: 10.1039/C8SC04228D
O=C(CCCN1CCC(c2ccccc2)(c2ccccc2)CC1)c1ccc(F)cc1
Reaction #415432
1-[3-(p-fluorobenzoyl)propyl] -4,4-diphenylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCI)c1ccc(F)cc1O
Reaction #432745
1-(4-fluoro-2-hydroxyphenyl)-4-iodo-1-butanone
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCI)c1ccc(F)cc1
Reaction #575051
desired compound
Ausbeute 96.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCC(=O)c1ccc(F)cc1)CC1CCN(Cc2ccccc2)CC1
Reaction #575052
desired compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COC2(CCN(CCCC(=O)c3ccc(F)cc3)CC2)CN1
Reaction #757431
DOI: 10.1039/C8SC04228D
O=C(CCCI)c1ccc(F)cc1
Reaction #765817
DOI: 10.1039/C8SC04228D
O=C(CCCI)c1ccc(F)cc1O
Reaction #933946
1-(4-fluoro-2-hydroxyphenyl)-4-iodo-1-butanone
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCI)c1ccc(F)cc1O
Reaction #1175552
1-(4-fluoro-2-hydroxyphenyl)-4-iodo-1-butanone
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CN2CN(c3ccccc3)C3(CCN(CCCC(=O)c4ccc(F)cc4)CC3)C2=O)c1
Reaction #1838178
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCI)c1ccc(F)cc1
Reaction #1838181
title compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1cccc(CN2CN(C3CCCCC3)C3(CCN(CCCC(=O)c4ccc(F)cc4)CC3)C2=O)c1
Reaction #1838261
product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1ccc(N2CN(c3ccccc3)C3(CCN(CCCC(=O)c4ccc(F)cc4)CC3)C2=O)cc1
Reaction #1838324
product
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCN1CCC(c2ccccc2)(c2ccccc2)CC1)c1ccc(F)cc1
Reaction #2249139
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(CN2CN(c3ccccc3)C3(CCN(CCCC(=O)c4ccc(F)cc4)CC3)C2=O)c1
Reaction #2450103
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCI)c1ccc(F)cc1
Reaction #2450106
title compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1cccc(CN2CN(C3CCCCC3)C3(CCN(CCCC(=O)c4ccc(F)cc4)CC3)C2=O)c1
Reaction #2450191
product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1ccc(N2CN(c3ccccc3)C3(CCN(CCCC(=O)c4ccc(F)cc4)CC3)C2=O)cc1
Reaction #2450256
product
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
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