子结构搜索

861

COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #471
收率 39.9%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #472
收率 58.1%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #473
收率 41.6%
CN(C)C(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #488
收率 51.2%
CN(C)C(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #489
收率 49.3%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #534
收率 66.2%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #535
收率 71.9%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #536
收率 67.3%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #537
收率 52.2%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #538
收率 65.9%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #539
收率 67.0%
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #540
收率 56.0%
CN(C)C(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #692
收率 33.8%
CC(Nc1cc(F)cc(F)c1F)c1cc(C(=O)N(C)C)cc2c(=O)cc(N3CCOCC3)oc12
Reaction #836
收率 83.0%
CCC[Si@H]1CC[C@H](c2cc(F)c(-c3cc(F)c(C(F)=CF)c(F)c3)c(F)c2)CC1
Reaction #2750
4'-(trans-4-n-propyl-4-silacyclohexyl)-2',6',3,5-tetrafluoro-4-(1,2-difluorovinyl)biphenyl
DOI: 10.6084/m9.figshare.5104873.v1
CCC[Si@H]1CC[C@H](c2ccc(-c3ccc(C(Cl)=CCl)cc3)cc2)CC1
Reaction #2751
4'-(trans-4-n-propyl-4-silacyclohexyl)-4-(1,2-dichlorovinyl)biphenyl
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(-c2ccsc2)cc(F)c1F
Reaction #3169
3(3,4,5-trifluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccsc2)cc1F
Reaction #3170
3(3,4-difluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(F)cc(-c2ccsc2)c1
Reaction #3171
3(3,5-difluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccsc2)c(F)c1
Reaction #3172
pure product
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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