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541700

CCCC(=O)c1ccccc1
Reaction #49840
ketone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1ccc(O)cc1O
Reaction #57513
solid
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc2c1Sc1ccccc1S2
Reaction #62072
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(Br)C(=O)c1ccsc1
Reaction #66704
2-Bromo-1-thiophen-3-yl-butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc3onc(C(F)(F)c4ccc5ncccc5c4)c3n2)sn1
Reaction #68616
product
Выход 3.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ncc(-c2ccc3nnc(CNC(=O)OC(C)(C)C)n3n2)s1
Reaction #68622
product
Выход 71.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)N1[C@H](C(O)CC)COC1(C)C
Reaction #80531
10a
DOI: 10.6084/m9.figshare.5104873.v1
CCC(Br)C(=O)c1ccsc1
Reaction #169023
2-Bromo-1-thiophen-3-yl-butan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Cc1ccc(OCc2ccccc2)cc1
Reaction #173122
DOI: 10.1039/C8SC04228D
CC(C)C(O)C1C(O[Si](C)(C)C(C)(C)C)CCN1C(=O)OC(C)(C)C
Reaction #173243
DOI: 10.1039/C8SC04228D
COc1cc(Br)c(F)cc1F
Reaction #173762
DOI: 10.1039/C8SC04228D
CC(C)Cc1csc2ccc(F)cc12
Reaction #173833
DOI: 10.1039/C8SC04228D
COc1cc(O)c(C2(O)C(=O)N(C(c3ccccc3)c3ccccc3)c3ccccc32)cc1C
Reaction #173967
DOI: 10.1039/C8SC04228D
CC(C)[Si](C#Cc1ccc(Cc2cc(Br)ccc2Cl)cc1)(C(C)C)C(C)C
Reaction #174045
DOI: 10.1039/C8SC04228D
Nc1cccc(Cl)c1C(O)Cc1ccc(F)c(F)c1
Reaction #174123
DOI: 10.1039/C8SC04228D
COc1ccc(CNC2(Cc3ccccc3)CCC3(CC2)OCCO3)cc1
Reaction #174222
DOI: 10.1039/C8SC04228D
N#Cc1ccc(C2(O)CCn3cncc32)cc1
Reaction #175016
DOI: 10.1039/C8SC04228D
CN(C)CCCC1(c2ccc(F)cc2)OCc2cc(C#N)ccc21
Reaction #175151
DOI: 10.1039/C8SC04228D
ClCc1ccc(Cl)cc1
Reaction #175303
DOI: 10.1039/C8SC04228D
CCCCCCC(O)c1ccccc1Br
Reaction #175576
DOI: 10.1039/C8SC04228D
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