Recherche de Sous-structure

C=CCBr

CC1(Br)C=C(Cl)C(F)=CN1
Reaction #1961
title compound
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCc1cc(Cl)c(F)cn1
Reaction #1962
title compound
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C(OC)C(C)Oc1ccc(Oc2ccc(Br)cc2F)cc1
Reaction #4557
product
Rendement 58.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(COC)C(=O)OCC
Reaction #10452
title compound
Rendement 28.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(CBr)Oc1cccc(Cl)c1F
Reaction #47332
4-bromo-3-(3-chloro-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester
Rendement 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)N1CC(Oc2cccc(Cl)c2F)=CC1=O
Reaction #47333
(S)-2-[4-(3-chloro-2-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid methyl ester
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(CBr)Oc1cc(F)ccc1F
Reaction #47357
4-bromo-3-(2,5-difluoro-phenoxy)-but-2-enoic acid ethyl ester
Rendement 87.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)N1CC(Oc2cc(F)ccc2F)=CC1=O
Reaction #47358
(S)-2-[4-(2,5-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid methyl ester
Rendement 17.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1cc(C)ccc1F
Reaction #47368
(E)-4-bromo-3-(2-fluoro-5-methyl-phenoxy)-but-2-enoic acid ethyl ester
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)N1CC(Oc2cc(C)ccc2F)=CC1=O
Reaction #47369
(S)-2-[4-(2-fluoro-5-methyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid methyl ester
Rendement 43.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O
Reaction #47480
(S)-3-cyclohexyl-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1ccccc1OC(C)C
Reaction #47485
(E)-4-bromo-3-(2-isopropoxy-phenoxy)-but-2-enoic acid ethyl ester
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2ccccc2OC(C)C)=CC1=O
Reaction #47486
(S)-3-cyclohexyl-2-[4-(2-isopropoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Rendement 29.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1ccccc1SC
Reaction #47490
(E)-4-bromo-3-(2-methylsulfanyl-phenoxy)-but-2-enoic acid ethyl ester
Rendement 38.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2ccccc2SC)=CC1=O
Reaction #47491
(S)-3-cyclohexyl-2-[4-(2-methylsulfanyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Rendement 12.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1cccc(F)c1F
Reaction #47509
(E)-4-bromo-3-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl ester
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(F)c2F)=CC1=O
Reaction #47510
(S)-3-cyclohexyl-2-[4-(2,3-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Rendement 26.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1cc(Cl)ccc1Cl
Reaction #47514
(E)-4-bromo-3-(2,5-dichloro-phenoxy)-but-2-enoic acid ethyl ester
Rendement 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cc(Cl)ccc2Cl)=CC1=O
Reaction #47515
(S)-3-cyclohexyl-2-[4-(2,5-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Rendement 15.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\CBr)Oc1ccccc1
Reaction #47573
(E)-4-bromo-3-phenoxy-but-2-enoic acid ethyl ester
Rendement 74.5%DOI: 10.6084/m9.figshare.5104873.v1
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