MgSO4

Cl.NCCCC[C@@H](N)C(=O)O
Reaction #891
D-lysine monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(CC)N=Cc1ccccc1
Reaction #945
desired product
收率 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OCc2ccccc2)CSC[C@H]1c1ccccc1
Reaction #1284
(3R-cis)-Tetrahydro-5-oxo-3-phenyl-6-[[(phenylmethoxy)carbonyl]amino]-1,4-thiazepine-4(5H)-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OCc2ccccc2)CSC[C@H]1c1ccccc1
Reaction #1418
(3R-cis)-Tetrahydro-5-oxo-3-phenyl-6-[[(phenylmethoxy)carbonyl]amino]-1,4-thiazepine-4(5H)-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCCN[C@@H]1CCCN(Cc2ccccc2)C1
Reaction #1711
title compound
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1
Reaction #5069
2-(Diphenylmethyl)-1-azabicyclo[2.2.2]octan-3-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)[C@@H](Cc1ccccc1)N=Cc1ccccc1
Reaction #6020
N-benzylidene-D-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(C2COC(=O)C2)cc1
Reaction #8296
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)[Si](C(C)C)(C(C)C)n1ccc2cc(Br)ccc21
Reaction #8432
5-Bromo-1-triisopropylsilyl-indole
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8526
title compound
收率 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8527
title compound
收率 95.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8528
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8529
title compound
收率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1CC[C@@H](Oc2cc(N)ccc2C(F)(F)F)C1
Reaction #8731
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)Nc1cccc2c1C(=O)CCC2
Reaction #9356
N-(8-oxo-5,6,7,8-tetrahydro-naphthalen-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #9362
oil
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C(=NC1CCN2CCCC2C1)c1ccncc1
Reaction #9969
title compound
收率 100.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NCCNCc1ccc(F)cc1
Reaction #11801
title compound
收率 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C(O)COc1ccccc1)[N+](=O)[O-]
Reaction #41354
subtitle compound
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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