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226979

CC(C)c1cccc(C(C)C)c1NC(=O)CBr
Reaction #1060
N-(2,6-diisopropylphenyl)-2-bromoacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C(C)C)c1N=Nc1cc(C(C)(C)C)cc(C(C)(C)C)c1O
Reaction #10702
phenol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N=Nc2c(C(C)C)cccc2C(C)C)c(O)c(-c2c3ccccc3cc3ccccc23)c1
Reaction #10703
phenol
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(c2ccccc2C=Nc2c(C(C)C)cccc2C(C)C)C(C)=C1C
Reaction #43987
N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethylene]-N-(2,6-diisopropylphenyl)amine
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1NS(=O)(=O)c1ccc(C)cc1
Reaction #54300
N-(2,6-diethylphenyl)-p-toluenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=N\c1c(C(C)C)cccc1C(C)C)c1cc(C)cc(Br)c1O
Reaction #73706
yellowish solid
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)c(O)c(/C(=N/c2c(C(C)C)cccc2C(C)C)c2ccccc2)c1
Reaction #73711
34
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C(C)C)c1N=C(c1ccccc1)c1cccc(Br)c1
Reaction #73730
title product 17
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=Nc1c(C(C)C)cccc1C(C)C)c1cccc(Br)c1
Reaction #73755
13
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=Nc2c(C(C)C)cccc2C(C)C)c2cccc(Br)c2)cc1
Reaction #73759
title product
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NCc2ccccn2)nc(Nc2c(C(C)C)cccc2C(C)C)c1C
Reaction #91449
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(Br)cc(C(C)C)c1N
Reaction #92817
4-bromo-2,6-diisopropylaniline
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1NC(=O)c1nn(C)c2c1CCc1cnc(N)nc1-2
Reaction #169132
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1NC(=O)c1nn(C)c2c1CCc1cnc(I)nc1-2
Reaction #169152
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1NC(=O)c1nn(C)c2c1CCc1cnc(N)nc1-2
Reaction #169154
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1NCC=O
Reaction #179755
DOI: 10.1039/C8SC04228D
CCc1cccc(CC)c1NCC(C)O
Reaction #188517
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCc1nnn(CC(=O)Nc2ccc(F)cc2F)n1
Reaction #195286
DOI: 10.1039/C8SC04228D
CC(C)c1cccc(C(C)C)c1N=Cc1cccc(-c2c(CNC(C)(C)C)ccc3ccccc23)n1
Reaction #201181
DOI: 10.1039/C8SC04228D
Cc1ccc(C)c2c1OCc1ccccc1C2C(=O)Nc1c(C(C)C)cccc1C(C)C
Reaction #202319
DOI: 10.1039/C8SC04228D
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