chloroform

ClCC1CCN(Cc2ccccc2)C1
Reaction #961
(3RS)-1-benzyl-3-chloromethyl pyrrolidine
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
Выход 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1Cc2ccccc2C[C@H](N)C1=O
Reaction #1415
(S)-1,3,4,5-Tetrahydro-4-amino-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc2c(n1C)CCN(C(=O)c1ccc([N+](=O)[O-])cc1)c1ccccc1-2
Reaction #1449
6-(4-nitrobenzoyl)-2,3-dimethyl-3,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCn1c(-c2ccccc2)nc(C(F)(F)F)cc1=O
Reaction #1551
3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
Выход 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1CSCCN1
Reaction #1569
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCN1CCC(Cc2cccc3c4ccccc4n(C(=O)O)c23)CC1
Reaction #1713
title compounds
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(CCl)ccc[n+]1[O-]
Reaction #1777
3-Chloromethyl-2-methylpyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1c(CCl)ccc[n+]1[O-]
Reaction #1783
2-ethyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)c1c(CCl)ccc[n+]1[O-]
Reaction #1786
2-isopropyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc[n+]([O-])c(C)c1CCl
Reaction #1789
2,4-dimethyl-3-chloromethylpyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ncc(F)c(Cl)c1Cl
Reaction #1955
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NC(C)(C)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1
Reaction #2003
(R)-α-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]-1H-indole-3-propanoic acid, benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(N)cc1
Reaction #2572
title compound
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)OC1C=CC(O[Si](C)(C)C(C)(C)C)C1
Reaction #2645
(-)-acetic acid 4-tert-butyldimethylsilyloxy-cyclopent-2-enyl ester
Выход 51.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1C=C[C@H](OC2CCCCO2)C1
Reaction #2646
(-)-acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl ester
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O[C@@H]1C=C[C@H](OC2CCCCO2)C1
Reaction #2648
title compound
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1C=C[C@H](OC(C)(C)C)C1
Reaction #2649
(-)-acetic acid cis-4-tert-butyloxy-cyclopent-2-enyl ester
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2650
title compound
Выход 101.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1C=C[C@H](OCc2ccccc2)C1
Reaction #2651
(-)-acetic acid cis-4-benzyloxy-cyclopent-2-enyl ester
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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