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[BH4-].[Na+]

N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)COc1ccc(C#N)cc1
Reaction #1019
desired product
Выход 27.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)ccc1OCC(C)N
Reaction #1020
desired product
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1021
desired product
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1034
( IX )
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CCC1c1cncc(Br)c1
Reaction #1140
5-bromo-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cncc(C2CCCN2)c1
Reaction #1142
5-bromo-3-(2-pyrrolidinyl)pyridine
Выход 72.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCOc1cnc(-c2ccc(C(C)O)cc2)nc1
Reaction #1256
2-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine
Выход 100.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Reaction #1271
Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3O)cc1
Reaction #1327
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=Cc2c(-c3ccccc3)cccc2C1O
Reaction #1353
desired product
Выход 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(CCl)c1ccsc1S(=O)(=O)NC(C)(C)C
Reaction #1536
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1ccc(N)cc1
Reaction #1688
white solid
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CO)s1
Reaction #1692
2-cyano-5-(hydroxymethyl)thiophene
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(S(=O)(=O)Nc2ccc3nsnc3c2)cc1
Reaction #1720
4-ethylamino-N-(2,1,3-benzothiadiazol-5-yl)-1-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc([C@H]2CC[C@H](O)CC2)cc1
Reaction #1742
trans-4-(4-Dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCC(c2ccccc2)CC1
Reaction #1744
4-phenylcyclohexanol
Выход 66.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc2c(c1)C(O)CC(C)(C)C2
Reaction #1780
5,6,7,8-tetrahydro-3,7,7-trimethylquinoline-5-ol
DOI: 10.6084/m9.figshare.5104873.v1
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