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333030

CC(C)(C)OC(=O)CC1=C2CCCC(C)(C)C2CCC1=O
Reaction #64852
tert.butyl 2-[5,5-dimethyl-2-oxo-2,3,4,4a,5,6,7,8-octahydronaphth-1-yl]acetate
Выход 52.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(Cl)C2C3CCC(O3)C12
Reaction #69939
5-chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 139.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(OCc2cnc(-c3ccc(Cl)cc3)[se]2)C2C3CCC(O3)C12
Reaction #69942
5-[2-(4-chloro-phenyl)-selenazol-5-ylmethoxy]-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 77.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1-c1ncc(C(C)OC2=CC(=O)C3C4CCC(O4)C23)s1
Reaction #69951
5-{1-[2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 73.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1csc(COC2=CC(=O)C3C4CCC(O4)C23)c1
Reaction #69959
5-(4-ethyl-thiophen-2-ylmethoxy)-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 88.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1=CC(=O)C2C3CCC(O3)C12
Reaction #69961
5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Выход 64.9%DOI: 10.6084/m9.figshare.5104873.v1
COC1=CCC(C)(C)CC1=O
Reaction #72863
title compound
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C1C(=O)C(OC)=CCC1(C)C
Reaction #72864
crude title compound
Выход 2084.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1=CC(C)(C)CCC1=O
Reaction #72867
title compound
Выход 45.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C1CC(C)(C)C=C(OC)C1=O
Reaction #72868
title compound
Выход 81.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(OCc2cnc(-c3ccc(Cl)cc3)[se]2)C2CCC1C2
Reaction #74181
4-[2-(4-chlorophenyl)selenazol-5-ylmethoxy]bicyclo[3.2.1]oct-3-en-2-one
Выход 63.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCC2=C1C(c1cccc([N+](=O)[O-])c1)C=C(C(F)(F)F)N2
Reaction #82715
title compound
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(c2cccc([N+](=O)[O-])c2)C2=C(CCCC2=O)NC1(O)C(F)(F)F
Reaction #82716
3-carboethoxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl) -4,6,7,8-tetrahydro-5(1H)-quinolone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCC2=C1C(c1cccc([N+](=O)[O-])c1)C(C(=O)O)C(O)(C(F)(F)F)N2
Reaction #82717
3-Carboxy-2-trifluoromethyl-2-hydroxy-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone
Выход 31.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccccc2)CCC(=O)C2CN(Cc3ccccc3)CC21
Reaction #83695
(3aRS,7SR,7aRS)-2-benzyl-7-methyl-7-phenyl-4-perhydroisoindolone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](C=O)[C@@H](CO[Si](C)(C)C(C)(C)C)O2)c(=O)[nH]c1=O
Reaction #83832
5'-O-tert-butyldimethylsilyl-3'-deoxy-3'-formylthymidine
Выход 69.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=C(CC[C@](C)(O)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C(=O)C(C)=CC1=O
Reaction #92092
(R,R,R)-2-allyl-3-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5-methyl-[1,4]benzoquinone
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92093
oil
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
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