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c1cc2c(cc1C1CN1)OCO2

COC(=O)C=C(C(=O)OC)N1CC1c1ccc2c(c1)OCO2
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DOI: 10.1039/C8SC04228D
c1cc2c(cc1C1CO1)OCO2
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3,4-methylenedioxyphenyloxirane
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
c1cnc2ncccc2c1
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1,8 naphthyridine
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c1cc2c(cc1C1CO1)OCO2
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DOI: 10.1039/C8SC04228D
c1cc2c(cc1C1CN1)OCO2
Reaction #1028968
DOI: 10.1039/C8SC04228D
COC(=O)C(F)=CC1(c2ccc3c(c2)OCO3)CC1
Reaction #1050988
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(cc1C1CC1)OCO2
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1-(3,4-methylenedioxyphenyl)-cyclopropane
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(cc1C1CC1)OCO2
Reaction #1051021
1-(3,4-methylenedioxyphenyl)cyclopropane
Ausbeute 143.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2C(=O)C=C(N3CC3c3ccc4c(c3)OCO4)C2O1
Reaction #1206145
DOI: 10.1039/C8SC04228D
CC1(C)CNC(c2ccc3c(c2)OCO3)C1
Reaction #1221217
DOI: 10.1039/C8SC04228D
CC1(C)CNC(c2ccc3c(c2)OCO3)C1
Reaction #1244850
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2ccc3c(c2)OCO3)N(c2ccc(C#N)c(Cl)c2)C1
Reaction #1244851
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(cc1C1CN1)OCO2
Reaction #1345311
15
Ausbeute 88.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C(C(=O)OC)N1CC1c1ccc2c(c1)OCO2
Reaction #1345314
26
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2C(=O)C=C(N3CC3c3ccc4c(c3)OCO4)C2O1
Reaction #1345317
54
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(cc1C1CN1)OCO2
Reaction #1555904
15
Ausbeute 88.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C(C(=O)OC)N1CC1c1ccc2c(c1)OCO2
Reaction #1555907
26
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2C(=O)C=C(N3CC3c3ccc4c(c3)OCO4)C2O1
Reaction #1555911
54
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C1=CCC(c2ccc3c(c2)OCO3)C1
Reaction #2148798
5-(Cyclopent-3-enyl)benzo[d][1,3]dioxole
Ausbeute 32.3%DOI: 10.6084/m9.figshare.5104873.v1
C1=CCC(c2ccc3c(c2)OCO3)C1
Reaction #2407833
DOI: 10.1039/C8SC04228D
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