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1250927

Cc1cc(O)cnc1F
Reaction #168830
6-fluoro-5-methylpyridin-3-ol
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CSC(Oc2cccc(-c3ccc(F)nc3)c2)C(OC(C)=O)C1OC(C)=O
Reaction #173281
DOI: 10.1039/C8SC04228D
CN1C(=O)C2(COc3cc4c(cc32)OCO4)c2c(-c3ccc(F)nc3)cccc21
Reaction #179370
DOI: 10.1039/C8SC04228D
CCc1nc2c(N)nc3cc(-c4ccc(F)nc4)cnc3c2n1CC(C)(C)O
Reaction #223036
DOI: 10.1039/C8SC04228D
N#Cc1ccc(-c2ccc(F)nc2)cc1
Reaction #229148
DOI: 10.1039/C8SC04228D
Fc1ccc(-n2ncnc2-c2cc3c(s2)-c2nc(-c4ccc(F)nc4)ccc2OCC3)c(F)c1
Reaction #235868
DOI: 10.1039/C8SC04228D
CCCCCC1CCC(c2ccc(-c3ccc(F)nc3F)cc2)CC1
Reaction #239554
DOI: 10.1039/C8SC04228D
NS(=O)(=O)c1ccc(Nc2ncc3ccc(-c4ccc(F)nc4)cc3n2)cc1
Reaction #245807
DOI: 10.1039/C8SC04228D
N#Cc1cccnc1-c1ccc(F)nc1
Reaction #259263
DOI: 10.1039/C8SC04228D
Cc1cc(O)cnc1F
Reaction #263712
DOI: 10.1039/C8SC04228D
O=c1[nH]ccc2c3[nH]c(-c4c(F)cccc4Cl)nc3c3ccc(-c4ccc(F)nc4F)cc3c12
Reaction #265149
DOI: 10.1039/C8SC04228D
CC(=O)OC1CSC(Oc2cncc(-c3ccc(F)nc3)c2)C(OC(C)=O)C1OC(C)=O
Reaction #265165
DOI: 10.1039/C8SC04228D
CCNC(=O)Nc1cc(-c2ccc(F)nc2)ccn1
Reaction #272820
DOI: 10.1039/C8SC04228D
CC(C)S(=O)(=O)NC1Cc2ccc(-c3ccc(F)nc3)cc2C1
Reaction #291804
DOI: 10.1039/C8SC04228D
Fc1cc(-c2ccc(Cl)cn2)cnc1F
Reaction #306459
5-(5-chloropyridin-2-yl)-2,3-difluoropyridine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](c2ccc(C)c(Cc3ccc(-c4ccc(F)nc4)s3)c2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #308184
1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3-(5-(6-fluoro-3-pyridyl)-2-thienylmethyl)-4-methylbenzene
Ausbeute 19.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](c2ccc(Cl)c(Cc3ccc(-c4ccc(F)nc4)s3)c2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #308198
1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-4-chloro-3-(5-(6-fluoro-3-pyridyl)-2-thienylmethyl)benzene
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C#N)C(c2ccc3[nH]nc(-c4ccc(F)nc4)c3c2)C(C#N)=C2COCCN12
Reaction #324592
title compound
Ausbeute 49.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1ccc(F)nc1
Reaction #339447
desired compound
Ausbeute 75.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1cc(-c2ccc3ncc4c(c3c2)n(-c2c(C)nn(C)c2C)c(=O)n4C)cnc1F
Reaction #370570
DOI: 10.1039/C8SC04228D
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