Bromoacetaldehyde diethyl acetal

CCOC(CN1CCC(C(=O)c2ccc(F)cc2)CC1)OCC
Reaction #2556
title compound
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(COc1ccccc1)OCC
Reaction #6531
2-phenoxyacetaldehyde diethyl acetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(COc1ccc(C2(C(=O)O)CC2)cc1)OCC
Reaction #46201
1-[4-(2,2-diethoxy-ethoxy)-phenyl]-cyclopropanecarboxylic acid
Выход 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCOCC(OCC)OCC
Reaction #50167
2-(4-methylbutyloxy)acetaldehyde diethylacetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Nc1nc(O)c2cc[nH]c2n1
Reaction #50298
2-amino-4 -hydroxy-7H-pyrrolo[2,3-d]pyrimidine
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)CNCC(OCC)OCC
Reaction #53318
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nccs1)OCO3
Reaction #53341
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(COc1ccc(Oc2ccccc2)cc1)OCC
Reaction #63554
4-phenoxyphenoxyacetaldehyde diethyl acetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1-c1nccs1
Reaction #66684
5-(2-Isopropyl-4-methoxy-5-thiazol-2-yl-phenoxy)-pyrimidine-2,4-diamine
Выход 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(Cc1cccc2c1Cc1ccccc1-2)OCC
Reaction #67391
Fluorenyl Acetaldehyde Diethylacetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(CC1C=Cc2ccccc21)OCC
Reaction #67392
Indenyl Acetaldehyde Diethylacetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(CC1C=CC=C1)OCC
Reaction #67393
Cyclopentadienyl Acetaldehyde Diethylacetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(Cn1cc2c(-c3ccc(F)cc3)c(-c3ccncc3)c(-c3ccc(F)cc3)nc2n1)OCC
Reaction #70865
2-(2,2-diethoxyethyl)-4,6-bis(4-fluorophenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(CSC1C=CCCCC1)OCC
Reaction #75015
3-[(2,2-diethoxyethyl)thio]-1-cycloheptene
Выход 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
C=CC[C@H](COCc1ccccc1)OCC(OCC)OCC
Reaction #155569
product
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCC(OCC(OCC)OCC)C1CC1
Reaction #155612
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=c1c2ccoc2ccn1CC(O)O
Reaction #156131
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)c1nccs1
Reaction #161909
#14
Выход 10.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(COc1cnc(Cl)c(Cl)c1)OCC
Reaction #168804
2,3-dichloro-5-(2,2-diethoxyethoxy)pyridine
Выход 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(COc1ccc(F)nc1)OCC
Reaction #168808
5-(2,2-diethoxyethoxy)-2-fluoropyridine
Выход 99.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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