子结构搜索

Cc1cccc(NN)c1C

Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #1178
hydrazine
收率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #1179
expected product
收率 93.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #206841
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCc2ccc(Cl)c(NN=C(c3ccccc3)c3ccccc3)c2CC1
Reaction #259800
DOI: 10.1039/C8SC04228D
C1=Cc2cccc3ccn(c23)-c2ccccc21.Cl
Reaction #416198
indolo[1,7ab][1]benzazepine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(C)c2c(c1C)C1(C)Cc3ccccc3C1=N2
Reaction #527050
9b,10-dihydro-6,7,9,9b-tetramethyl-8-methoxyindeno[1,2-b]indole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NNC2=NCCS2)c1C
Reaction #569864
2-[2-(2,3-dimethylphenyl)-hydrazino]-2-thiazoline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(N=NC2=NCCS2)c1C
Reaction #569866
2-(2,3-dimethylphenylazo)-2-thiazoline
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)[C@@H]1Cc2c(C(C)=O)ccc3c2[C@H](CN3)C1
Reaction #573965
oil
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #652991
hydrazine
收率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #652992
expected product
收率 93.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #669942
hydrazine
收率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc(S(=O)(=O)O)c2c1CCCC2
Reaction #669944
expected product
收率 77.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #669946
expected product
收率 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1Cc2c(NN)ccc(Cl)c2C1=O.Cl
Reaction #738093
[7-chloro-2-(1-methylethyl)isoindolin-1-on-4-yl]hydrazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1Cc2c(NC=C3NCCCN3)ccc(Cl)c2C1=O
Reaction #738094
subject compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cc(S(=O)(=O)O)c(N)c3c2C(=O)c2ccccc2C3=O)c(C)c(S(=O)(=O)O)c(C)c1N(NCCN)c1ncnc(Cl)n1
Reaction #829026
solution 1
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NN(Cc2ccccc2)C(=O)OC(C)(C)C)c1C
Reaction #1041088
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCc2ccc(Cl)c(NN=C(c3ccccc3)c3ccccc3)c2CC1
Reaction #1100281
title compound
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1c(-c2cc(C(N)=O)n(C)c2)cccc1N1C(=O)c2ccc(C(C)(C)C)cc2CN1C
Reaction #1112761
2-(6-tert-butyl-3-methyl-1-oxo-3,4-dihydrophthalazin-2(1H)-yl)-6-(5-carbamoyl-1-methyl-1H-pyrrol-3-yl)benzyl acetate
收率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
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