子结构搜索

48

Fc1cc(Br)cc(F)n1
Reaction #8400
4-bromo-2,6-difluoropyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccnc(Cl)c1
Reaction #48060
2-chloro-4-trimethylsilanylethynyl-pyridine
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(C)cncc3C)cc(=O)oc2c1OC1CCCC1
Reaction #48919
8-(cyclopentyloxy)-4-(3,5-dimethylpyridin-4-ylamino)-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cc(C=O)ccn2)cc1
Reaction #50538
4-formyl-2-(4-methylphenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)n1c(-c2cccc(CO)c2)cc2c(Br)ccnc21
Reaction #57186
title compound
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)CC1
Reaction #57201
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]c(C(=O)O)cc23)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #57227
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2c(Br)ccnc2n1S(=O)(=O)c1ccccc1
Reaction #57230
title compound
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)c1
Reaction #57233
title compound
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)CC1
Reaction #57277
title compound
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)c1cc2c(Br)ccnc2n1S(=O)(=O)c1ccccc1
Reaction #57281
title product
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(Br)c(F)cn1
Reaction #68850
4-Bromo-2-ethoxy-5-fluoropyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnccc1Br
Reaction #69895
4-bromonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnccc1Br
Reaction #69896
4-bromonicotinic acid methyl ester
收率 45.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccnc(Br)c1
Reaction #71052
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccnc(Br)c1
Reaction #71078
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(-c2cc(Br)ccn2)c1
Reaction #71530
4-bromo-2-(3′-bromophenyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(Br)cc(Br)c1OCc1ccccc1
Reaction #77706
15
收率 90.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccc(Br)cc1=O
Reaction #84950
Ethyl (4-bromo-2-oxopyridin-1(2H)-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84951
Ethyl {4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}acetate
DOI: 10.6084/m9.figshare.5104873.v1
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