部分構造検索

12036

N[C@@H]1CCCC[C@@H]1C(=O)O
Reaction #7115
(1S,2R)-2-aminocyclohexanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #7116
crude product
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1N
Reaction #7119
(1S,2R)-2-aminocyclohexanecarboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7124
(1S,2S)-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7125
product
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[O-].[Na+].[Na+]
Reaction #40488
Na2CO3
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CCCC[C@H]1C(=O)O
Reaction #54524
cis-2-(dimethylamino)cyclohexanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CCCC[C@H]1N.Cc1ccc(S(=O)(=O)O)cc1
Reaction #70811
(1S,2R)-ethyl 2-aminocyclohexanecarboxylate tosylic acid
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCC2(C[C@@H]1C(=O)O)OCCO2)c1ccccc1
Reaction #70815
(7S,8R)-8-benzamido-1,4-dioxaspiro[4.5]decane-7-carboxylic acid
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC[C@@H](NC(=O)c2ccccc2)[C@@H](C(=O)O)C1
Reaction #70816
(1S,2R)-2-benzamido-5-oxocyclohexanecarboxylic acid
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(C)CC1N=[N+]=[N-]
Reaction #160356
2-Azido-4-methyl-cyclohexanecarboxylic acid ethyl ester
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1CCCC[C@@H]1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162134
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)[C@H]1CCCC[C@@H]1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162135
(1S,2S)-isopropyl 2-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@]1(C(=O)OC)CCCC[C@@H]1NC(=O)OCc1ccccc1
Reaction #162137
desired product ( 38b )
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)C2CCC1N2C(=O)OC(C)(C)C
Reaction #168304
7-tert-butyl 2-methyl 3-oxo-7-azabicyclo[2.2.1]heptane-2,7-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCCCC2NC(=O)OC(C)(C)C)CC1c1ccc(Cl)c(Cl)c1
Reaction #184782
DOI: 10.1039/C8SC04228D
Cc1cc(COc2ccc(S(=O)(=O)NC3CCCCC3C(=O)NO)cc2)c2ccccc2n1
Reaction #190209
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC1(C)C(C)CCN(C)C1C
Reaction #190749
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(NC(C)(C)C)CCC1N1CCC(N)C1=O
Reaction #197330
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCCCC1N(C(=O)CC1=NS(=O)(=O)c2cc(NS(C)(=O)=O)ccc2N1)C1CCCCC1
Reaction #199965
DOI: 10.1039/C8SC04228D
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