dicyclopropylmethanone

CC(C)(C)S(=O)N=C(C1CC1)C1CC1
Reaction #181558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(-c2ccccc2)cc1
Reaction #260902
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC(c1nccs1)(C1CC1)C1CC1
Reaction #288675
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=CC(c1cccc(Cl)c1)C(NC(C1CC1)C1CC1)c1ccc(Cl)cc1
Reaction #376801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN1Cc2c(C#CC(O)(C3CC3)C3CC3)ncn2-c2cccc(Cl)c2C1=O
Reaction #408877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)[S@@](=O)N=C(C1CC1)C1CC1
Reaction #497679
(R)—N-(dicyclopropylmethylidene)-2-methylpropane-2-sulfinamide
Ausbeute 22.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
OC(c1nccs1)(C1CC1)C1CC1
Reaction #497713
dicyclopropyl(1,3-thiazol-2-yl)methanol
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C=CC1CC(C(=O)OCC)=C(c2ccccc2)O1
Reaction #549762
4-carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
C=C[C@H](c1cccc(Cl)c1)[C@H](NC(C1CC1)C1CC1)c1ccc(Cl)cc1
Reaction #1019215
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
C=CC1CC(C(=O)OCC)=C(c2ccccc2)O1
Reaction #1067546
4-carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_01
CC(C)(C)[S@@](=O)N=C(C1CC1)C1CC1
Reaction #1127169
(R)—N-(dicyclopropylmethylidene)-2-methylpropane-2-sulfinamide
Ausbeute 22.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
OC(c1nccs1)(C1CC1)C1CC1
Reaction #1127203
dicyclopropyl(1,3-thiazol-2-yl)methanol
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
C=C[C@H](c1cccc(Cl)c1)[C@H](NC(C1CC1)C1CC1)c1ccc(Cl)cc1
Reaction #1135526
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
C=CC1CC(C(=O)OCC)=C(c2ccccc2)O1
Reaction #1292902
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
OC(c1cccc(S)c1)(C1CC1)C1CC1
Reaction #1293993
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
OC(c1cnc(Sc2ccc3c(ccc4nnc(-c5ccccc5)n43)c2)s1)(C1CC1)C1CC1
Reaction #1312709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
—
Reaction #1577779
DOI: 10.1021/ja400103pBorylation dataset from Roche
—
Reaction #1577788
DOI: 10.1021/ja400103pBorylation dataset from Roche
CN1Cc2c(C#CC(O)(C3CC3)C3CC3)ncn2-c2cccc(Cl)c2C1=O
Reaction #1694173
7-chloro-3-(3,3-dicyclopropyl-3-hydroxy-1-propynyl)-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_09
CC(C)(C)c1cc(C(=O)C=C(C2CC2)C2CC2)cc(C(C)(C)C)c1O
Reaction #1808544
3,5-di-tert-butyl-4-hydroxyphenyl-3,3-dicyclopropylprop-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
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