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8669

OC(CCCc1ccccc1)CCCc1ccccc1
Reaction #975
alcohol
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1)C(O)CCCc1ccccc1
Reaction #978
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1ccc(CCCC(O)CCCc2ccccc2)cc1)(c1ccccc1)c1ccccc1
Reaction #988
alcohol
Ausbeute 122.9%DOI: 10.6084/m9.figshare.5104873.v1
OCC#CC1CCCCC1
Reaction #2165
3-cyclohexyl-2-propyn-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3cccc4ccccc34)sc2c1
Reaction #2287
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccc4ccccc4c3)sc2c1
Reaction #2289
title compound
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)c1ccc(OC)c(OC2CCCC2)c1
Reaction #2445
product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)c1ccc(OC)c(OC2CCc3ccccc32)c1
Reaction #2446
product
Ausbeute 9.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)[PH](=O)C(C)CCC
Reaction #2455
di-2-pentylphosphine oxide
Ausbeute 52.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCC(O)(CCCCCCCCCC)CCCCCCCCCC
Reaction #2684
di-n-decyl-n-tetradecylcarbinol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCC(O)(CCCCCCCCCC)CCCCCCCCCCCCCC
Reaction #2686
n-nonadecyl-n-tetradecyl-n-decylcarbinol
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1ocnc1C
Reaction #2893
4-Methyl-5-propionyloxazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)C(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #3186
3β-acetoxy-24-oxo-5-cholestene
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC12CCCN1CCC2
Reaction #3396
oil
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #4352
desired product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)N[C@@H](CC(C)C)C(=O)CCC(C)C
Reaction #4353
desired product
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(O)(CCC(C)C)[C@H](CC(C)C)NS(=O)(=O)c1ccccc1C
Reaction #4354
desired product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #4355
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1noc(COc2ccc(Cl)cc2Cl)n1
Reaction #4993
desired product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
OC(CC1CCN(CC2CC2)CC1)(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #5236
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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