子结构搜索

C=CCBr

CC1(Br)C=C(Cl)C(F)=CN1

收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1

CNCc1cc(Cl)c(F)cn1

收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C=C(OC)C(C)Oc1ccc(Oc2ccc(Br)cc2F)cc1

收率 58.2%DOI: 10.6084/m9.figshare.5104873.v1

C=C(COC)C(=O)OCC

Reaction #10452

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 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

收率 74.5%DOI: 10.6084/m9.figshare.5104873.v1

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