EtOH

CCCCCCC(O)CCCCCCCCCCCOCC(O)CNCCO
Reaction #1190
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)COCC(O)CNCCO
Reaction #1191
title compound
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC(CC)COCCCCCCCCCCOCC(O)CNCCO
Reaction #1194
title compound
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCOC(=O)CCCCCCCCCCCOCC(O)CNCCO
Reaction #1195
title compound
Ausbeute 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[Si](C)(C)CCCCCCCCCCCOCC(O)CNCCO
Reaction #1197
title compound
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCOCC(C)(O)CNCCO
Reaction #1199
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCOCC(O)CNCCCO
Reaction #1200
title compound
Ausbeute 135.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCOCC(C)(O)CCNCCO
Reaction #1201
title compound
Ausbeute 30.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1204
title compound
Ausbeute 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCC(O)CN(C)CCO
Reaction #1205
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCOCC(NCCO)C(C)(C)O
Reaction #1206
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1209
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCSCC(O)CNCCO
Reaction #1213
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCC(=O)OCC(O)CN(C)CCO
Reaction #1214
title compound
Ausbeute 60.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(=O)C(=NO)C(=O)c1c(C)cc(C)cc1C
Reaction #1249
semi-solid
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
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc(N)c(N)c(Cl)n1
Reaction #1263
desired product
Ausbeute 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1282
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Cc1ccc(Br)cc1
Reaction #1303
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(I)cc1
Reaction #1318
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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