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58909

CC(C)(C)[Si](C)(C)OC[C@@H]1CC(=O)[C@H]1CO[Si](C)(C)C(C)(C)C
Reaction #6046
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON=C1C[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H]1CO[Si](C)(C)C(C)(C)C
Reaction #6047
title compound
Выход 75.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCC1CC(O)C1CO[Si](C)(C)C(C)(C)C
Reaction #6052
title compound
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC(CO)C1=O)c1ccccc1
Reaction #6055
title compound
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC(CO)C1O)c1ccccc1
Reaction #6056
title compound
Выход 101.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2C(O)CCC12
Reaction #43463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCC2C(=O)CC12)c1ccccc1
Reaction #43464
title compound
Выход 86.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2C(CCC2OC(=O)c2ccccc2)N1
Reaction #43465
1J
Выход 133.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CC(C)C1
Reaction #48328
1-Allyl-3-methylcyclobutanol
Выход 46.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64370
[1S-(1α,2β,3β)]-3-hydroxy-1,2-cyclobutanedimethanol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64371
[1S-(1α,2β,3β)]-3-hydroxy-1,2-cyclobutanedimethanol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64372
[1S-(1α,2β,3β)]-3-hydroxy-1,2-cyclobutanedimethanol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2CCC3CCC1C32
Reaction #78831
2-oxatricyclo[5.2.1.04,10]decane-3-one
Выход 617.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(C2=C(O)C(C)(c3ccccc3)C2=O)c2ccccc2)sc2ccccc12
Reaction #207177
DOI: 10.1039/C8SC04228D
CC1(C)CC(=O)C1(Cl)CC(Cl)(Cl)Cl
Reaction #214358
2-chloro-2-(2',2',2'-trichloroethyl)-3,3-dimethylcyclobutan-1-one
Выход 60.2%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC=CC1CC2=O
Reaction #227481
DOI: 10.1039/C8SC04228D
O=C1CC2CCCCC12
Reaction #231717
DOI: 10.1039/C8SC04228D
OC1C2CCC=CC2C1(Cl)Cl
Reaction #238053
DOI: 10.1039/C8SC04228D
O=C(OC1CC(CO)C1O)c1ccccc1
Reaction #241280
DOI: 10.1039/C8SC04228D
O=C(OC1CC(CO)C1=O)c1ccccc1
Reaction #246480
DOI: 10.1039/C8SC04228D
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