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992177

COC1=NC(C(C)C)C(OC)=NC1CCC(F)(F)F
Reaction #159198
2-Isopropyl-3,6-dimethoxy-5-(3,3,3-trifluoro-propyl)-2,5-dihydro-pyrazine
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=NC(C(C)C)C(OC)=NC1CCOCC(F)(F)F
Reaction #159204
2-Isopropyl-3,6-dimethoxy-5-[2-(2,2,2-trifluoro-ethoxy)-ethyl]-2,5-dihydro-pyrazine
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(CCOCC(F)(F)F)C(=O)OC
Reaction #159205
2-Methoxycarbonylamino-4-(2,2,2-trifluoro-ethoxy)-butyric acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC1=N[C@H](C(C)C)C(OC)=N[C@H]1Cc1ccc2ncccc2c1
Reaction #161997
6-{[(2S,5R)-3,6-dimethoxy-5-(propan-2-yl)-2,5-dihydropyrazin-2-yl]methyl}quinoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)Cc1ccc2ncccc2c1
Reaction #161998
methyl (2S)-2-amino-3-(quinolin-6-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC1=N[C@H](C(C)C)C(OC)=N[C@H]1Cc1cc(-c2ccc(Cl)s2)on1
Reaction #163979
(2S,5R)-2-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-isopropyl-3,6-dimethoxy-2,5-dihydro-pyrazine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)Cc1cc(-c2ccc(Cl)s2)on1
Reaction #163980
(S)-2-Amino-3-[5-(5-chloro-thiophen-2-yl)-isoxazol-3-yl]-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=N[C@H](C2CCCCC(=O)C2)C(OCC)=N[C@H]1C(C)C
Reaction #164511
title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=NC(C(C)C)C(OC)=NC1CCC(F)(F)F
Reaction #167140
2-Isopropyl-3,6-dimethoxy-5-(3,3,3-trifluoro-propyl)-2,5-dihydro-pyrazine
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=NC(C(C)C)C(OC)=NC1CCOCC(F)(F)F
Reaction #167146
2-Isopropyl-3,6-dimethoxy-5-[2-(2,2,2-trifluoro-ethoxy)-ethyl]-2,5-dihydro-pyrazine
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(CCOCC(F)(F)F)C(=O)OC
Reaction #167147
2-Methoxycarbonylamino-4-(2,2,2-trifluoro-ethoxy)-butyric acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC1=NC(C(C)C)C(OC)=NC1CC1CC(F)C(O[Si](C)(C)C(C)(C)C)C1
Reaction #178500
DOI: 10.1039/C8SC04228D
CCCCCc1nc2cc(CCC3(C)N=C(OC)C(C(C)C)N=C3OC)ccc2o1
Reaction #187166
DOI: 10.1039/C8SC04228D
COC1=NC(C(C)C)C(OC)=NC1Cc1ccccc1OC(F)(F)F
Reaction #193255
DOI: 10.1039/C8SC04228D
COC1=N[C@H](Cc2ccc(C(F)(F)F)cc2F)C(OC)=N[C@H]1C(C)C
Reaction #220011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1=N[C@H](Cc2cc(F)c(F)cc2F)C(OC)=N[C@H]1C(C)C
Reaction #220012
title compound
Выход 62.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1=N[C@H](Cc2ccc(C(F)(F)F)cc2F)C(OC)=N[C@H]1C(C)C
Reaction #220239
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1=N[C@H](Cc2cc(F)c(F)cc2F)C(OC)=N[C@H]1C(C)C
Reaction #220240
title compound
Выход 62.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1=NC(C(C)C)C(OC)=NC1Cc1cc(F)c(F)cc1F
Reaction #222755
DOI: 10.1039/C8SC04228D
COC(=O)NC(CCOCC(F)(F)F)C(=O)OC
Reaction #242530
DOI: 10.1039/C8SC04228D
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