benzene

CCCCCCCCCCCC
Reaction #863
dodecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCC(O)C1CO1
Reaction #1216
1,2-epoxy-3-tridecanol
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CNNC(=O)OC(C)(C)C
Reaction #1290
[2-[(1,1-Dimethylethoxy)carbonyl]hydrazino]acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1309
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC1(O)CCC(C)(C)c2cc(C#Cc3ccc(C(=O)OCC)cc3)ccc21
Reaction #1333
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(CC=Cc1ccccc1Br)(C(=O)O)C(=O)O
Reaction #1357
desired product
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CNNC(=O)OC(C)(C)C
Reaction #1424
[2-[(1,1-dimethylethoxy)carbonyl]hydrazino]acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1463
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCOC(=O)C1(O)CCC(C)(C)c2ccc(/C=C/c3ccc(C(=O)OCC)cc3)cc21
Reaction #1469
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC1=CCC(C)(C)c2ccc(N=Nc3ccc(C(=O)OCC)cc3)cc21
Reaction #1478
title compounds
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1482
EtOAc-hexanes
Выход 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC1=CCC(C)(C)c2cc(C(C)=O)ccc21
Reaction #1483
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC1(O)CCC(C)(C)c2ccc(Br)cc21
Reaction #1494
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1496
EtOAc-hexanes
Выход 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC[Si@H]1CC[C@H](/C=C/C#Cc2ccc(F)cc2)CC1
Reaction #1499
desired product
Выход 15.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
Reaction #1647
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC#CCOC(=O)C1CN=CNC1
Reaction #1694
5-(2-butynyloxycarbonyl)-1,4,5,6-tetrahydropyrimidine
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(CNC2CCCc3ccc(OCc4ccncc4)cc32)cc1
Reaction #1707
Compound 12
Выход 97.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1Nc2ccc(Cl)cc2C1(c1ccccc1)c1ccccc1
Reaction #1911
5-Chloro-1,3-dihydro-3,3-diphenylindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CC(C)(C)NC(=O)OCc1ccccc1
Reaction #1999
product
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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