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615880

CC(C)(C)NC(=O)c1ccccc1C(C(=O)C(C)(C)C)c1ccccc1
Reaction #75090
N-tert.butyl-α-phenyl-α-pivaloyl-o-toluamide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1OC)C(C)(C)C(=O)CC2
Reaction #90170
title compound
Rendimiento 91.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)O
Reaction #177656
DOI: 10.1039/C8SC04228D
CCOC(=O)CN1N=C(C2CCCCC2)c2ccccc2N(CC(=O)C(C)(C)C)C1=O
Reaction #192957
DOI: 10.1039/C8SC04228D
CCC(CC)(c1ccc(OCC(=O)C(C)(C)C)c(C)c1)c1cc2cc(OS(C)(=O)=O)ccc2o1
Reaction #195012
DOI: 10.1039/C8SC04228D
COC(=O)CNC(=O)C1=C(O)c2cc(Cl)ccc2C2(CCN(C(=O)c3ccccc3)CC2)C1=O
Reaction #196120
DOI: 10.1039/C8SC04228D
CC1(C)C(=O)C(C(=O)NCC(=O)O)=C(O)c2cc(Cl)cc(F)c21
Reaction #197311
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCCC1CCCC1=O
Reaction #197637
DOI: 10.1039/C8SC04228D
O=C(O)CNC(=O)C1=C(O)c2cc(Cl)ccc2C2(CCC2)C1=O
Reaction #202614
DOI: 10.1039/C8SC04228D
CCCCC12CCc3c(cc(F)c(OC)c3Cl)C1=CC(=O)C2
Reaction #203697
DOI: 10.1039/C8SC04228D
COC(=O)CNC(=O)C1=C(O)c2cc(Cl)ccc2C2(CCOCC2)C1=O
Reaction #204909
DOI: 10.1039/C8SC04228D
O=C(O)CNC(=O)C1=C(O)c2ccc(Cl)cc2C2(CCOCC2)C1=O
Reaction #206562
DOI: 10.1039/C8SC04228D
CC(=O)C1(c2ccccc2)CCN(CCCCC23CCCc4cccc(c42)NC3=O)CC1
Reaction #211301
DOI: 10.1039/C8SC04228D
CC(C)OC(OC(C)C)C(C)(C)C(=O)C(C)C(OC(=O)OCC(Cl)(Cl)Cl)C(C)COCc1ccccc1
Reaction #218797
32a
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(COCc1ccccc1)C(OC(=O)OCC(Cl)(Cl)Cl)C(C)C(=O)C(C)(C)C=O
Reaction #218798
67
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(OC(C)C)C(C)(C)C(=O)C(C)C(OC(=O)OCC(Cl)(Cl)Cl)C(C)COCc1ccccc1
Reaction #218802
desired product
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)C(Oc1cccc(F)n1)n1ccnc1
Reaction #223729
DOI: 10.1039/C8SC04228D
CCC(CC)(c1ccc(OCC(=O)C(C)(C)C)c(C)c1)c1cc2ccc(OS(C)(=O)=O)cc2o1
Reaction #225901
DOI: 10.1039/C8SC04228D
CC(C)(C)C(=O)CN1C(=O)N(CC(=O)Nc2cccc(NCC(=O)O)c2)N=C(C2CCCCC2)c2ccccc21
Reaction #231270
DOI: 10.1039/C8SC04228D
CC1(c2cccc(O)c2)C(=O)Nc2cc(Cl)cc(Cl)c2C1=O
Reaction #237114
DOI: 10.1039/C8SC04228D
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