Substructure Search

C=C

COC(=O)Cn1c(C(=O)N[C@H](CCCCNC(=O)C=Cc2ccccc2)C(=O)NCCCCCc2c(OC)cc(C)cc2OC)cc2ccccc21
Reaction #3024
methyl (R)-{2-[N-{1-[(2,6-dimethoxy-4-methylphenyl)pentylcarbamoyl]-5-(cinnamoylamino)pentyl}carbamoyl]indol-1-yl}acetate
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(C(=O)OCc2ccccc2)N(C(=O)OC(C)(C)C)C1
Reaction #7736
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CNN(C(=O)OCc2ccccc2)C1
Reaction #7737
desired product
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42260
solid
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42261
solid
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42266
solid
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42267
solid
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45532
solid
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45533
solid
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45538
solid
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45539
solid
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(/C=C/c1ccc(Cl)c(C(F)(F)F)c1)=NO
Reaction #50645
(E)-4-chloro-3-trifluoromethylcinnamamide oxime
Yield 40.1%DOI: 10.6084/m9.figshare.5104873.v1
N#CC=Cc1ccc(Cl)c(C(F)(F)F)c1
Reaction #50646
4-chloro-3-trifluoromethyl-cinnamonitrile
Yield 87.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CN(C(=O)OCc2ccccc2)N(C(=O)OC(C)(C)C)C1
Reaction #50944
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CNN(C(=O)OCc2ccccc2)C1
Reaction #50945
desired product
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CN(C(c2ccccc2)c2ccccc2)C1)c1cccc(O)c1
Reaction #53455
1-benzhydryl-3-[(3-hydroxyphenyl)(methylsulfonyl)methylene]azetidine
Yield 28.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CN(C(c2ccccc2)c2ccccc2)C1)c1ccc(O)cc1
Reaction #53456
1-benzhydryl-3-[(4-hydroxyphenyl)(methylsulfonyl)methylene]azetidine
Yield 44.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CN(C(c2ccccc2)c2ccccc2)C1)c1cccc(CO)c1
Reaction #53461
1-benzhydryl-3-[(3-hydroxymethylphenyl)(methylsulfonyl)methylene]azetidine
Yield 57.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2[nH]c(C)c(N)c12
Reaction #80291
desired product
Yield 79.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82736
title compound
Yield 55.2%DOI: 10.6084/m9.figshare.5104873.v1
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