Teilstruktursuche

57722

Cc1cc(-c2cc(-c3nc4ccc(Cl)cc4n3COCC[Si](C)(C)C)c(=O)n(COCC[Si](C)(C)C)n2)cc(C)c1O
Reaction #40552
4-[6-Chloro-1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-6-(4-hydroxy-3,5-dimethyl phenyl)-2-(2-trimethylsilanylethoxymethyl)-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(B2OC(C)(C)C(C)(C)O2)cc(C)c1OC(=O)c1oc2ccccc2c1C
Reaction #57730
3-methyl-benzofuran-2-carboxylic acid 2,6-dimethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl ester
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(B2OC(C)(C)C(C)(C)O2)cc(C)c1OCCOS(C)(=O)=O
Reaction #59035
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)ccc1-c1cc(C)c(OCCN[C@@H](C)[C@H](O)c2ccc(O)cc2)c(C)c1
Reaction #59048
title compound
Ausbeute 22.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=CCN(C(=O)OC(C)(C)C)CC2)cc(C)c1O
Reaction #89780
desired product
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1c(C)cc(B2OC(C)(C)C(C)(C)O2)cc1C
Reaction #189090
DOI: 10.1039/C8SC04228D
CCCOc1c(C)cc(-c2ccc3c4c([nH]c3c2F)-c2ccc(C(=O)OC)cc2CC4)cc1C
Reaction #206292
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2cc(C)c(O)c(C)c2)cc1
Reaction #309259
desired product
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(-c3nc4ccc(Cl)cc4n3COCC[Si](C)(C)C)c(=O)n(COCC[Si](C)(C)C)n2)cc(C)c1O
Reaction #377156
DOI: 10.1039/C8SC04228D
Cc1cc(C(=O)O)ccc1-c1cc(C)c(OCCNC(C)C(O)c2ccc(O)cc2)c(C)c1
Reaction #405699
DOI: 10.1039/C8SC04228D
CCC(=O)c1cc(-c2cc(C)c(O)c(C)c2)nnc1OC
Reaction #406558
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2cc(C)c(O)c(C)c2)cc1
Reaction #473815
desired product
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cnc2ccc(-c3cc(C)c(O)c(C)c3)nc2c1N[C@H]1CC[C@H](CN(C)C)CC1.[Cl-].[Cl-]
Reaction #613304
desired product
Ausbeute 95.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=CCN(C(=O)OC(C)(C)C)CC2)cc(C)c1O
Reaction #622292
desired product
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(-n3cccn3)cc2)c(C#N)c(C)c1O
Reaction #716555
title compound
Ausbeute 22.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(-c3ccn(C)n3)cc2)c(C)c(C)c1O
Reaction #716576
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(-n3cccn3)cc2)c(C)c(C)c1O
Reaction #716585
title compound
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(-n3cccn3)cc2F)c(C)c(C)c1O
Reaction #716591
title compound
Ausbeute 91.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(Cl)cc2)c(C)c(C)c1O
Reaction #716595
title compound
Ausbeute 71.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(OC)cc2)c(C)c(C)c1O
Reaction #716598
title compound
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter