ethyl chloroformate

COc1ccncc1NC(=O)c1c[nH]c2c1C(=O)CCC2
Reaction #1006
N-(4-methoxy-3-pyridyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole 3-carboxamide
Выход 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[C@@H]1COC(=O)N1
Reaction #1395
(R)-4-tert-butyl-2-oxazolidinone
Выход 80.0%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
Выход 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C(=O)OC(C)(C)C)c1cccc(N=C=O)c1
Reaction #2437
title compound
Выход 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1ccc(CO)cc1
Reaction #2543
title compound
Выход 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)NCc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2603
title compound
Выход 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2604
title compound
Выход 37.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]ccc2sccc12
Reaction #2856
title compound
Выход 49.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1Cc2ccccc2C1=O
Reaction #3494
2-carbethoxy-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Cc1ccc(C(=O)c2ccccc2)cc1[N+](=O)[O-]
Reaction #4569
ethyl 2-nitro-4-benzoylphenylacetate
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)OC(=O)N1C[C@H](O)C[C@H]1C(N)=O
Reaction #5162
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #5167
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)C(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #5173
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCNC(=O)[C@@H]1C[C@H](O)CN1C(=O)OC(C)(C)C
Reaction #5194
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)SC[C@H]1CCCCCC[C@H](C(N)=O)NC1=O
Reaction #5492
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)NCCC1(O)CCc2ccccc2C12CCCC2
Reaction #5637
title compound
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C(NCc1cccc(C(F)(F)F)c1)c1cn(C(=O)OCC)c2ccccc12.Cl
Reaction #5702
title compound
Выход 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)OC(=O)OCC
Reaction #5845
diethyl pyrocarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1c(Cl)ccc2c1C1CCCCC1O2
Reaction #5980
1-amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC1(C)CCC(C)(C)c2cc(OCc3ccc(CO)cc3)ccc21
Reaction #6609
title compound
Выход 37.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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