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312

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #202
Выход 35.7%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #204
Выход 31.5%
CC(C)(C)OC(=O)NCCC1CCN(c2ccccc2)CC1
Reaction #317
Выход 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(O)cc1
Reaction #760
Выход 0.0%
C[C@@H]1CN(c2ccc(S(C)(=O)=O)cc2)CCN1C(=O)OC(C)(C)C
Reaction #787
Выход 0.0%
FC1(F)Oc2ccc(N3CCNCC3)cc2O1
Reaction #802
Выход 50.7%
COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #813
Выход 90.5%
COC(=O)[C@H](Cc1ccccc1)n1cc(-c2cccc3ccccc23)cc(NC(=O)c2ccc(C(F)(F)F)cc2)c1=O
Reaction #7903
title compound
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)ccc1OCC(=O)O
Reaction #9436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3cccc(C(F)(F)F)c3)cc2)c2ccc(-c3cccc(C(F)(F)F)c3)cc2)ccc1OCC(=O)O
Reaction #9438
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)ccc1OCC(=O)O
Reaction #9439
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2cc3ccccc3cc2c1
Reaction #9799
Anthracene
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cnn(C(=O)OC(C)(C)C)c2)cc1C=O
Reaction #10791
4-(5-formyl-2,4-dimethoxy-phenyl)-pyrazole-1-carboxylic acid tert-butyl ester
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(C2CC=CO2)c1
Reaction #10843
3-(2,3-dihydro-furan-2-yl)-benzaldehyde
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(C2C=CCO2)cc1C=O
Reaction #10845
5-(2,5-dihydro-furan-2-yl)-2,4-dimethoxy-benzaldehyde
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCC)c1nc(OC)c(F)cc1NC(=O)OC(C)(C)C
Reaction #43408
1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)/C=C/c1cc(CO[Si](C)(C)C(C)(C)C)cc(OC)n1
Reaction #43626
desired product
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3cccc(CO)c3)c(C(=O)Nc3ccccc3)n2)cc1
Reaction #48601
4-(3-hydroxymethyl-phenyl)-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Выход 131.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(/C=C/c2cccc3c4c([nH]c23)C2CCN(CC2)C4)cn1
Reaction #66064
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C#Cc2cccc3c4c([nH]c23)C2CCN(CC2)C4)cn1
Reaction #66066
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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