Поиск подструктуры

C1C2C=CC(C1CO)O2

Cc1cc(OCc2ccccc2)cc(C)c1C1=C(OC(=O)C(C)(C)C)C2C3C=CC(O3)C2C1=O
Reaction #1280214
rac-(1R,2S,6R,7S)-4-(4-benzyloxy-2,6-dimethylphenyl)-5-oxo-10-oxatricyclo[5.2.1.02,6]deca-3,8-dien-3-yl 2,2-dimethylpropionate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(CCO)C(=O)N1
Reaction #1355270
hydroxy ethylmaleimide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)C2C3C=CC(O3)C2C(=O)O)cc1
Reaction #1508702
3-(4-Methoxyphenylsulfonyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC12CCC(S(=O)(=O)c3ccccc3)(O1)C(C(=O)NOCc1ccccc1)C2
Reaction #1508703
4-Methoxyphenylsulfonyl-7-oxabicyclo[2.2.1]heptane-2-carboxylic acid benzyloxyamide
DOI: 10.6084/m9.figshare.5104873.v1
OCC1CC2C=CC1O2
Reaction #1519100
7-oxanorborn-2-en-5-ylmethanol
DOI: 10.6084/m9.figshare.5104873.v1
BrCC1CC2C=CC1O2
Reaction #1519101
7-oxanorborn-2-en-5-yl-methyl bromide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2c(O)cccc21
Reaction #1529655
product 7
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2C3C=CC(O3)C12
Reaction #1569914
3a,4,7,7a-tetrahydro-4,7-epoxyisobenzofuran-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(O3)C2C(=O)N1CCO
Reaction #1569915
2-(2-hydroxyethyl)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2C3C=CC(O3)C12
Reaction #1586507
desired product
Выход 87.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(O3)C2C(=O)N1CCO
Reaction #1586508
desired product
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1C[C@@H]2C=C[C@H]1O2
Reaction #1591574
(1R,2R,4R)-ethyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate
Выход 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1C[C@@H]2CC[C@H]1O2
Reaction #1591575
(1R,2R,4S)-ethyl 7-oxabicyclo[2.2.1]heptane-2-carboxylate
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2C3C=CC(O3)C2C(=O)N1CCO
Reaction #1634111
DOI: 10.1039/C8SC04228D
COC(=O)C1CC2C=CC1O2
Reaction #1671219
2-carbomethoxy-7-oxabicyclo(2.2.1)hept-5-ene
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OC
Reaction #1671220
methylacrylate
Выход 292.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C1CC2C=CC1O2
Reaction #1671221
2-carbobutoxy-7-oxabicyclo(2.2.1)hept-5-ene
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C2C=CC(O2)C1C(=O)OCC
Reaction #1683161
light brown liquid
Выход 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=CCCCCC(C)C(=O)[O-].O=C1C=CC(=O)O1
Reaction #1683317
dodec-7-ene-2-carboxylate maleic anhydride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=CCCCCC(C)C(=O)[O-].O=C1C=CC(=O)O1
Reaction #1683318
dodec-7-ene-2-carboxylate maleic anhydride
DOI: 10.6084/m9.figshare.5104873.v1
НазадСтраница 2Далее