بحث البنية الفرعية

1433522

COC(=O)CCc1ccc(C#N)cc1
Reaction #1687
colorless oil
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Cc2cccc(OC)c2C1C(=O)OCC
Reaction #5441
desired product
المردود 96.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1C(C#N)C(C#N)CC2
Reaction #5448
desired product
المردود 85.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(S(=O)(=O)C[C@@H]2C[C@H](N)CC[C@@H]2NC(=O)OC(C)(C)C)cc1
Reaction #7775
(1S*,2R*,4R*)-[4-amino-2-(4-methylsulfanyl-benzenesulfonylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester
المردود 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncsc1CCC(=O)C(C)C
Reaction #51723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1Oc2ccc(C(C)C(=O)OC)cc2C(=O)C1C
Reaction #54964
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)ONS(=O)(=O)c1cccc(N)c1
Reaction #57424
product
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(Oc2ccncc2)CC(C(=O)NO)C1C(=O)N1CCC(c2ccccc2)CC1
Reaction #89727
titled compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](OC(=O)N2CCCC2)C[C@H](C(=O)NO)[C@H]1C(=O)N1CCC(c2ccccc2)CC1
Reaction #89736
product
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H](N)C(=O)O
Reaction #164023
L-tert-leucine
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(F)cc1F
Reaction #318856
2,4-difluorobenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]cnc1CC1CCc2cccnc2C1=O
Reaction #339264
7-((5-Methyl-1H-imidazol-4-yl)methyl)-6,7-dihydroquinolin-8(5H)-one
المردود 5920.8%DOI: 10.6084/m9.figshare.5104873.v1
[Ba+2].[Cl-].[Cl-]
Reaction #344483
barium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].CC(=O)[O-].[Ba+2]
Reaction #344484
barium acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].CC(=O)[O-].[Ba+2]
Reaction #344485
barium acetate
DOI: 10.6084/m9.figshare.5104873.v1
[Ba+2].[Cl-].[Cl-]
Reaction #344486
barium chloride
DOI: 10.6084/m9.figshare.5104873.v1
[Ba+2].[Cl-].[Cl-]
Reaction #344487
barium chloride
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c3c(cccc3c1N1CCCCC1)C(=O)N(O)C2=O
Reaction #366200
title compound
المردود 45.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(C#N)cc3c4c(cccc24)C(=O)N(O)C3=O)C1
Reaction #366202
(S)-[1-(5-cyano-2-hydroxy-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-6-yl)-pyrrolidin-3-yl]-carbamic acid, tert-butyl ester
المردود 42.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)NO)cc1
Reaction #366899
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي