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546741

CN(C)C(CCc1ccccc1)C1CCC(=O)CC1
Reaction #40922
ketone
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc(C(=O)NC2C3CC4CC(C3)CC2C4)c1NCCO
Reaction #41116
5-(2-Hydroxy-ethylamino)-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
DOI: 10.6084/m9.figshare.5104873.v1
COCCNc1c(C(=O)NC2C3CC4CC(C3)CC2C4)cnn1C
Reaction #41124
5-(2-Methoxy-ethylamino)-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1(C(N)c2ccccc2)CCCCC1
Reaction #49100
title compound
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1NCC2CCCCC21
Reaction #52154
octahydroisoindole-1-carboxylic acid
Выход 131.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2CCCCC2CN1S(=O)(=O)c1cc(Cl)cc(Cl)c1
Reaction #52155
N-(3,5-dichlorobenzenesulfonyl)-octahydro-isoindole-1-carboxylic acid
Выход 192.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)N2CC3CCCCC3C2C(=O)O)cc1
Reaction #52162
N-(4-methylbenzenesulfonyl)-octahydroisoindole-1-carboxylic acid
Выход 62.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(CO)C1CCCCC1
Reaction #56778
tert-butyl 1-cyclohexyl-2-hydroxyethylcarbamate
Выход 66.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #69116
solid
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3nc(N[C@H](C)C4CCC(O)CC4)ncc3C#N)c3cc(C(F)(F)F)cnc32)cc1
Reaction #69117
title compound
Выход 88.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)OC(C)(C)C)C1CCC(O)CC1
Reaction #69128
title compound
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)OC(C)(C)C)[C@H]1CC[C@@H](OS(C)(=O)=O)CC1
Reaction #69129
compound
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)C(=O)N[C@H]1CC[C@H]([C@@H](C)NC(=O)OC(C)(C)C)CC1
Reaction #69130
title compound
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)C(=O)N[C@H]1CC[C@H]([C@@H](C)N)CC1
Reaction #69131
desired compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)C(=O)N[C@H]1CC[C@H]([C@@H](C)Nc2ncc(C#N)c(-c3c[nH]c4ncc(C(F)(F)F)cc34)n2)CC1
Reaction #69132
title compound
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)[C@@]1(c2ccccc2)C[C@@H]2C[C@H]1CC2Oc1cc2cc[nH]c(=O)c2cc1Cl
Reaction #73471
desired product
Выход 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(O)CC1
Reaction #73482
4-(1-Amino-1-phenyl-ethyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CC1
Reaction #73483
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)N[C@H](CO)C1CCCCC1
Reaction #86830
(S)-2-(1-cyclohexyl-2-hydroxyethylamino)-2-oxoacetic acid
Выход 56.5%DOI: 10.6084/m9.figshare.5104873.v1
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