ethyl N-ethoxycarbonyliminocarbamate

COC(=O)c1ccc(OC(=O)C2CCOCC2)cc1OC
Reaction #1770
methyl 4-(4-tetra-hydropyranoyloxy)-2-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(OC(=O)[C@@H]2CCCC[C@@H]2c2ccccc2)cc1OC
Reaction #1773
methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(OC(=O)C2CCOc3ccccc32)cc1OC
Reaction #1778
methyl 4-(4-chromanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(OC(=O)[C@H]2CC[C@@H](NC(=O)OC(C)(C)C)CC2)cc1OC
Reaction #1790
methyl 4-[N-Boc-cis-1-amino-4-cyclohexanoyloxy]-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(OC(=O)c2cc(=S(=O)=O)cco2)cc1OC
Reaction #1793
methyl 4-[4-sulfonylpyranoyloxy]-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC
Reaction #2341
methyl 4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]-3-vinylbutyrate
Выход 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(CN2C(=O)CCC2=O)cc1
Reaction #2570
title compound
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccccc1)c1ccccc1SSc1ccccc1C(=O)c1ccccc1
Reaction #3842
title compound
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)SC1CNC(=O)C1
Reaction #5215
4-acetylthio-2-pyrrolidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(CC=Cc1ccc(Cl)cc1)CCN(CCN1CCCCC1)S(=O)(=O)c1cccc2cnccc12
Reaction #5841
title compound
Выход 74.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOP(=O)(CO[C@@H](COn1cnc2c(OC)nc(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)nc21)CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)OCC
Reaction #6361
(S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-(t-butyldiphenylsilyloxy)-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurine
Выход 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOP(=O)(CO[C@@H](COCc1ccccc1)COn1cnc2c(OC)nc(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)nc21)OCC
Reaction #6365
(S)-2-[bis-(t-butoxycarbonyl)amino]-9-[3-benzyloxy-2-(diethoxyphosphorylmethoxy)propoxy]-6-methoxypurine
Выход 88.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1cccc(O[C@H](CCCl)c2ccccc2)c1
Reaction #8488
product
Выход 15.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)CC3CC3)c(SC)nn12
Reaction #9317
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCC1(CN2C(=O)c3ccccc3C2=O)CCN(Cc2ccccc2)C1
Reaction #10454
title compound
Выход 21.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)Oc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11715
title compound
Выход 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1c2ccccc2C(=O)N1C[C@H]1CO1
Reaction #40656
desired product
Выход 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)CCOc1ccc(-n2ccc(OCc3ccccc3)cc2=O)cc1
Reaction #43311
title compound
Выход 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(OC2CCSCC2)cc(C)c1Br
Reaction #43903
title compound
Выход 86.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46153
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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