部分構造検索

885

Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
Reaction #541
収率 40.2%
Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
Reaction #542
収率 10.4%
Oc1ccc(I)cc1OCc1ccccc1
Reaction #90507
2-(benzyloxy)-4-iodophenol
収率 62.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccc(O)c(OCc2ccccc2)c1)C(=O)OCc1ccccc1)OCc1ccccc1
Reaction #90508
(S)-benzyl 3-(3-(benzyloxy)-4-hydroxyphenyl)-2-(((benzyloxy)carbonyl)amino)propanoate
収率 104.0%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(I)cc1OCc1ccccc1
Reaction #173306
DOI: 10.1039/C8SC04228D
C[Si](C)(C)CCN1C(=O)CN(c2ccc(CC3NC(=O)c4ccccc4-c4ccccc43)cc2OCc2ccccc2)S1(=O)=O
Reaction #176366
DOI: 10.1039/C8SC04228D
CC(C)(CC#N)Cc1ccc(N2CC(=O)N(CC[Si](C)(C)C)S2(=O)=O)c(OCc2ccccc2)c1
Reaction #177788
DOI: 10.1039/C8SC04228D
Ic1cccc(OCc2ccccc2)c1
Reaction #179019
DOI: 10.1039/C8SC04228D
C[Si](C)(C)CCN1C(=O)CN(c2ccc(CCC(F)(F)F)cc2OCc2ccccc2)S1(=O)=O
Reaction #179177
DOI: 10.1039/C8SC04228D
O=C1CN(c2ccc(-c3ccccc3)cc2OCc2ccccc2)S(=O)(=O)N1
Reaction #179806
DOI: 10.1039/C8SC04228D
COc1cc(C#N)c(I)cc1OCc1ccccc1
Reaction #189605
DOI: 10.1039/C8SC04228D
CCCOc1c(I)cc(C(=O)CCC(=O)OCC)cc1OCc1ccccc1
Reaction #192070
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-n2ccnc2)cc1OCc1ccccc1
Reaction #209545
DOI: 10.1039/C8SC04228D
CCCCS(=O)(=O)Oc1ccc(CC=Cc2ccc(C=CC(=O)OC)c(OCc3ccccc3)c2)cc1OC
Reaction #212250
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC(Cc2ccc(N3CC(=O)N(CC[Si](C)(C)C)S3(=O)=O)c(OCc3ccccc3)c2)C1
Reaction #223568
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(I)cc(OCc2ccccc2)c1
Reaction #224867
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-n2cccn2)cc1OCc1ccccc1
Reaction #227198
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CNc1ccc(I)cc1OCc1ccccc1
Reaction #229410
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCc1ccc(N2CC(=O)N(CC[Si](C)(C)C)S2(=O)=O)c(OCc2ccccc2)c1
Reaction #229657
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(I)cc1OCc1ccccc1
Reaction #237040
DOI: 10.1039/C8SC04228D
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