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CCOC(=O)C=P(c1ccccc1)(c1ccccc1)c1ccccc1

CCOC(=O)CCCc1cccc(Br)c1
Reaction #1302
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCc1ccc(Br)cc1
Reaction #1306
ethyl 4-(4-bromophenyl)but-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #1452
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCc1ccc(Br)cc1
Reaction #1461
ethyl 4-(4-bromophenyl)but-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1C(=O)[C@@H](C/C=C/C(=O)O)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1883
trans-7-chloro-5-(2-chlorophenyl)-1-isopropyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-crotonic acid
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc(=O)c(OCc2ccccc2)c[nH]1
Reaction #4212
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(/C=C/C(=O)OCc3ccccc3)cc2c1
Reaction #11106
benzyl (2E)-3-(5-methoxy-1H-indol-2-yl)-2-propenoate
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1OC(=O)c2c(Oc3nc(OC)cc(OC)n3)cccc21
Reaction #50446
3-(ethoxycarbonylmethyl)-7[(4,6-dimethoxy-pyrimidin-2-yl)oxy]-phthalide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(C(F)(F)CCC(=O)O)cc2)cc1
Reaction #52037
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #52833
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCc1ccc(Br)cc1
Reaction #52842
ethyl 4-(4-bromophenyl)but-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(CC(=O)O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55201
3-(2',4'-difluoro-4-biphenylyl)butyric acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)C1C(Sc2ccccc2)CC2CC(=O)N21
Reaction #56011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56020
( 123 )
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCCNC(=O)c1[nH]c2ccc(F)cc2c1I
Reaction #58064
5-[(5-fluoro-3-iodo-1H-indole-2-carbonyl)-amino]-pent-2-enoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1CC(c2cccc(Br)c2)C1
Reaction #58876
[3-(3-bromophenyl)cyclobutylidene]acetic acid ethyl ester
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C)=C/c1cc(F)c(F)c(F)c1
Reaction #73966
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #81581
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCc1ccc(Br)cc1
Reaction #81585
ethyl 4-(4-bromophenyl)but-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #81645
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
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