Sodium borohydride

N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1034
( IX )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1C(=O)CCC1c1cncc(Br)c1
Reaction #1140
5-bromo-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Brc1cncc(C2CCCN2)c1
Reaction #1142
5-bromo-3-(2-pyrrolidinyl)pyridine
收率 72.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1cnc(-c2ccc(C(C)O)cc2)nc1
Reaction #1256
2-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine
收率 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3O)cc1
Reaction #1327
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC1=Cc2c(-c3ccccc3)cccc2C1O
Reaction #1353
desired product
收率 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NCc1ccc(N)cc1
Reaction #1688
white solid
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(CO)s1
Reaction #1692
2-cyano-5-(hydroxymethyl)thiophene
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)Cc1ccc([C@H]2CC[C@H](O)CC2)cc1
Reaction #1742
trans-4-(4-Dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC1CCC(c2ccccc2)CC1
Reaction #1744
4-phenylcyclohexanol
收率 66.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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.v1uspto-grants-1998_03
O=S(=O)=c1cc(O)cco1
Reaction #1792
sulfonylpyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(CNc2ccc(Cl)cc2C(O)c2ccccc2Cl)c(OC)c1
Reaction #1868
5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol
收率 96.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1[C@@H](CCCO)O[C@H](c2ccccc2)c2ccccc2N1Cc1ccccc1
Reaction #1876
trans-1-benzyl-3-(3-hydroxypropyl)-5-phenyl-1,5-dihydro-4,1-benzoxazepin-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccc(Br)cc1C(O)c1ccccn1
Reaction #1897
2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)CN1C(=O)[C@@H](CCO)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1900
trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-ethanol
收率 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(OCc2ccccc2)ccc1C(O)c1cc(Cl)ccc1N
Reaction #1904
2-amino-α-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcohol
收率 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(Cc1ccc(C(O)c2ccc(Cl)cc2)cc1)C(F)(F)F
Reaction #2199
desired product
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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