Substructure Search

C1CCCC(CCC1)O

C=C(C)C#N.C=C(C)C(=O)O.CC(=CC12CC3CC(CC(C3)C1C)C2)C(=O)[O-].CCC1OC1=O
Reaction #8657
2-methyladamantanylmethacrylate methacrylonitrile alpha-butyrolactone Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CC3CC(C2)CC1C3
Reaction #9839
2-adamantanon
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC(=O)C(=O)Nc2c(C(C)C)cccc2C(C)C)c(O)c(C23CC4CC(CC(C4)C2)C3)c1
Reaction #11832
solid
Yield 48.4%DOI: 10.6084/m9.figshare.5104873.v1
C1CCCC2OC2CC1
Reaction #42012
9-oxabicyclo[6.1.0] nonane
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCC(O)CCC1
Reaction #44492
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CCCC(O)CCC2)CC1CO
Reaction #44496
titled product
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H](C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #46043
(αS)-α-amino-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46046
IV
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](C(=O)N1[C@H](C#N)C[C@@H]2C[C@@H]21)C12CC3CC(CC(O)(C3)C1)C2
Reaction #46049
3-cyano-(αS)-α-(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl)-β-oxo-(1S,3S,5S)-2-azabicyclo[3.1.0]hexane-2-ethanecarbamic acid, 1,1-dimethylethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Br)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57408
α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Br)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57409
α-bromo-3-hydroxytricyclo [3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57410
a-amino-3-hydroxytricyclo[3.3.1.1 3,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H](C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #57412
(S)-amino-(3-hydroxy-adamantan-1-yl)-acetic acid
Yield 105.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC12CC3CC(CC(C3)C1)C2)c1ccc([N+](=O)[O-])cc1
Reaction #62818
1-adamantyl 2-(p-nitrophenyl)propionate
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC12CC3CC(CC(C3)C1)C2)c1ccc(N)cc1
Reaction #62819
1-adamantyl 2-(p-aminophenyl)propionate
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC12CC3CC(CC(C3)C1)C2)c1ccc2nc(N)sc2c1
Reaction #62820
1-adamantyl 2-amino-α-methylbenzothiazole-6-acetate
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(c2ncc[nH]2)C23CC4CC(CC(C4)C2O)C3)cc1
Reaction #64189
4-[2-hydroxy-adamant-1-yl-1-(imidazolyl)methyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(N)C2CC3CC1CC(O)(C3)C2
Reaction #66726
title compound
Yield 76.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC12CC3CC(C1)C(O)C(C3)C2)OCc1ccccc1
Reaction #66731
desired product
Yield 53.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(OC(=O)COC(=O)CO)C2CC3CC(C2)CC1C3
Reaction #72403
objective compound
Yield 67.1%DOI: 10.6084/m9.figshare.5104873.v1
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