cyclopentene

Cc1cc(C2C=CCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N
Reaction #2988
N-diaminomethylene-2-methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl[Si](Cl)(Cl)C1CCCC1
Reaction #6540
Cyclopentyl trichlorosilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl[Si](Cl)(Cl)C1CCCC1
Reaction #6543
Cyclopentyl trichlorosilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl[Si](Cl)(Cl)C1CCCC1
Reaction #6545
Cyclopentyl trichlorosilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl[Si](Cl)(Cl)C1CCCC1
Reaction #6547
Cyclopentyl trichlorosilane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1C2=C(CCC2)[C@H]2CCC[C@@H]12
Reaction #10585
cis-tricyclo [6.3.0.03,7] undec-1(8)-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2CCCC12
Reaction #75690
Compound 59
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CN1CC2CCCC2c2ccccc21
Reaction #257459
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C2C=CCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N
Reaction #388191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cl[Si](Cl)(Cl)C1CCCC1
Reaction #405482
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1C2=C(CCC2)[C@H]2CCC[C@@H]12
Reaction #409098
cis-tricyclo[6.3.0.03,7]undec-1(8)-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COC(=O)CC1C(OC(C)=O)CC(=O)C1C(=O)OC
Reaction #415932
2-Carbomethoxy-3-Oxo-5-Acetoxycyclopentaneacetic Acid Methyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
OCc1ccccc1C1CCCC1
Reaction #456969
2-cyclopentylbenzyl alcohol
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
OCc1cccc(C2CCCC2)c1
Reaction #456972
3-cyclopentylbenzyl alcohol
Ausbeute 232.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(C)(C)OC(=O)[C@@H](N)Cc1ccc(O)c(C2CCCC2)c1
Reaction #456989
tert-butyl 3-cyclopentyl-L-tyrosinate
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCOC(=O)[C@@H](N)Cc1ccc(N)cc1C1CCCC1
Reaction #456996
ethyl 4-amino-2-cyclopentyl-L-phenylalaninate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC1(C)CC(=O)C2C3CCCC3C2(C)C1
Reaction #458783
5,5,7-trimethyltricyclo[6.3.0.02,7 ]undecane-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
OCc1cccc(C2CCCC2)c1
Reaction #517079
3-cyclopentylbenzyl alcohol
Ausbeute 232.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)(C)OC(=O)[C@@H](N)Cc1ccc(O)c(C2CCCC2)c1
Reaction #517096
tert-butyl 3-cyclopentyl-L-tyrosinate
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCOC(=O)[C@@H](N)Cc1ccc(N)cc1C1CCCC1
Reaction #517104
ethyl 4-amino-2-cyclopentyl-L-phenylalaninate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
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