LiAlH4

CC=CCC(N)(CC)CO
Reaction #946
desired product
المردود 32.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCC1CCN(Cc2ccccc2)C1
Reaction #963
product
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #968
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1[C@@H]1CN(Cc2ccccc2)C[C@H]1CO
Reaction #1166
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc([C@H]2CN(Cc3ccccc3)C[C@H]2CO)c(O)c1
Reaction #1167
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCC(O)CCCCCCCCCCCO
Reaction #1189
1,12-octadecanediol
المردود 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCC=CCCCCCCCCNCCO
Reaction #1207
title compound
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCCCCCCCCCCCCCCCCN(CCO)CCO
Reaction #1211
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1ccc(-c2ccc(CO)cc2)cc1
Reaction #1523
4-hydroxymethyl-4'-decyloxybiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCn1c(-c2ccccc2)nc(CC)c(CCO)c1=O
Reaction #1556
6-ethyl-5-(2-hydroxyethyl)-2-phenyl-3-propargyl-4(3H)-pyrimidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCc1cc(OCc2ccccc2)ccc1O
Reaction #1617
4-benzyloxy-2-hydroxymethyl phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCCN[C@@H]1CCCN(Cc2ccccc2)C1
Reaction #1711
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1ncccc1CO
Reaction #1781
2-ethyl-3 -hydroxymethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)c1ncccc1CO
Reaction #1784
2-isopropyl-3-hydroxymethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccnc(C)c1CO
Reaction #1787
2,4-dimethyl-3-hydroxymethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc2c(c1)CN(c1ccc(OCCN3CCCCC3)cc1)C1=C2CCc2cc(OC)ccc21
Reaction #1809
title compound
المردود 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(OC)c(C(O)c2cc(Cl)ccc2N)c(OC)c1
Reaction #1886
crystal
المردود 96.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC(c1ccccc1Cl)c1cc(Cl)ccc1NCC(F)(F)F
Reaction #1890
oily compound
المردود 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
FC(F)(F)CNC1CCN(Cc2ccccc2)C1
Reaction #1980
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1985
title compound
المردود 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي