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86892

CC(C)(C)OC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10046
[2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-ylmethyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CNC(C)=O)c1C(=O)OC
Reaction #10047
product
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10048
product
Выход 22.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CNC(=O)OCc2ccccc2)c1C(=O)OC
Reaction #10052
product
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)OCc4ccccc4)c3C2=O)C(=O)N1
Reaction #10053
product
Выход 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(COCC(C)(C)CO)c1C(=O)OC(C)(C)C
Reaction #43372
tert-Butyl 2-(3-hydroxy-2,2-dimethylpropoxymethyl)-6-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(COCCCCO)c1C(=O)OC(C)(C)C
Reaction #43373
tert-Butyl 2-(4-hydroxybutoxymethyl)-6-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2cc(-c3cccc4c3C(=O)OC4=O)ccc21
Reaction #59817
a-BPDA
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(O)c(C(=O)OC)c(C(=O)OC)c1C
Reaction #61280
desired product
Выход 88.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(O)c(C(=O)OC)c(C(=O)OC)c1C
Reaction #61941
desired product
Выход 88.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cc(CC)c(C)c(C(=O)OC)c1C(=O)OC
Reaction #61942
desired product
Выход 83.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=S)c2cccc(-c3ccccc3)c21
Reaction #69387
3-phenylthio-phtalic anhydride
Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c2c[nH]cc2c1
Reaction #69752
6-methoxy-4-methyl-isoindole
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=S)c2cccc(-c3ccccc3)c21
Reaction #71015
3-phenylthio-phtalic anhydride
Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)C(F)(F)F)c(C)c1C(=O)O
Reaction #87631
desired title product
Выход 56519.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)C(F)(F)F)c(C)c1C(N)=O
Reaction #87632
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(C(=O)O)c1C(=O)O
Reaction #89599
Benzene Tricarboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])cc(C(=O)O)c1C(=O)O
Reaction #94503
5-nitro-1,2,3-benzenetricarboxylic acid
Выход 50.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)c([N+](=O)[O-])cc2c1C(=O)N(CCN(C)C)C2=O
Reaction #156537
designed compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)c(OC)cc(O)c1C=O
Reaction #173323
DOI: 10.1039/C8SC04228D
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