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C1COC1

CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #790
Ausbeute 23.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #791
Ausbeute 11.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #792
Ausbeute 3.5%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C
Reaction #824
Ausbeute 16.5%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #832
Ausbeute 7.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #833
Ausbeute 0.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #834
Ausbeute 8.7%
C=CCC[C@H](OC(=O)[C@H](C)NC=O)[C@H]1OC(=O)[C@H]1CCCCCC
Reaction #6159
N-formyl-L-alanine (S)-1-[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl)-4-pentenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(COCCCCBr)COC1
Reaction #7425
3-[(4-bromobutoxy)methyl]-3-ethyloxetane
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(COCCCCOc2ccc(C(=O)O)cc2)COC1
Reaction #7426
4-[7-(3-ethyl-3-oxetanyl)-1,6-dioxaheptyl]benzoic acid
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)CC3CCO3)c(SC)nn12
Reaction #9310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCC1(COCCOC)COC1
Reaction #63242
required monomer
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(N)cc2Br)COC1
Reaction #67471
3-bromo-4-(3-methyloxetan-3-yl)aniline
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C=C(C(=O)OC(C)(C)C)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)COC1
Reaction #85151
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-ethyloxetan-3-yl)prop-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC(C(=O)OC(C)(C)C)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)COC1
Reaction #85152
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-ethyloxetan-3-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC(C(=O)O)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)COC1
Reaction #85153
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1ccc(NC(=O)C(CC2(C)COC2)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85166
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC(C(=O)Nc2ccc(-c3noc(=O)[nH]3)cc2)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)COC1
Reaction #85318
2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-ethyloxetan-3-yl)-N-[4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]propanamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(CC2(C)COC2)C(=O)Nc2ccc(C(=O)O)cc2)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCCNCC2)nc(-n2ncc3cnc(-c4cnn(CC5COC5)c4)cc32)c1
Reaction #86138
solid
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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