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C1CCC(CC1)Cl

O=S(=O)(C1=CC2CCC1c1ccccc12)c1ccccc1
Reaction #10249
1,4-dihydro-2-phenylsulfony-1,4-ethanonaphthalene
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCCC(Cl)C1=O
Reaction #40300
2-tert-butyl-6-chlorocyclohexanone
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C1CCCC(Cl)C1=O
Reaction #40303
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Cl)CCCC1Cc1ccccc1
Reaction #40304
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CCCC(Cl)C1=O
Reaction #40305
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Cl)CCCC1c1ccccc1
Reaction #40306
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCCC(Cl)C1=O
Reaction #40307
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCC1CCCC(Cl)C1=O
Reaction #40308
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCC(Cl)C1=O
Reaction #40309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CC(c2ccccc2)CC(Cl)C1=O
Reaction #40335
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ClC1(Cl)CCC2OC2(Cl)C1
Reaction #50099
epoxide
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Cl)C1
Reaction #50102
liquid
DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(F)Cl
Reaction #50103
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(F)C1
Reaction #50104
epoxide
DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(Cl)Br
Reaction #50106
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Br)C1
Reaction #50107
epoxide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C(Cl)(Cl)CCC2OC21Cl
Reaction #50108
epoxide
Ausbeute 95.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1C(Cl)(Cl)CCC2OC21Cl
Reaction #50109
epoxide
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C(Cl)(Cl)CCC2OC21Cl
Reaction #50110
epoxide
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)cccc1Cl
Reaction #50111
phenol
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
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