3,3-dimethyldioxirane

Cc1c(C2CO2)c(OCc2ccc(F)cc2F)c(Br)c(=O)n1-c1c(F)cccc1F

Reaction #196117

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction #256242

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction #331952

8-Benzyloxy-3-methyl-5-oxiranyl-1H-quinolin-2-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)C/C=C\[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #341641

(E)-9,10-dehydroepothilone B

Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01

CCCCCCCCCCCC(=O)OC1CC(c2ccccc2)N(O)C(c2ccccc2)C1

Reaction #344858

title compound

Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11

CCCCCCCCCCCC(=O)OC1CC(c2ccccc2)N(O)C(c2ccccc2)C1C

Reaction #344860

title compound

Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11

CCCCCCCCCCCC(=O)OC1C(C)C(c2ccccc2)N(O)C(c2ccccc2)C1C

Reaction #344862

title compound

Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11

CCCCCCCCCCCC(=O)NC1C(C)C(c2ccccc2)N(O)C(c2ccccc2)C1C

Reaction #344864

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11

Reaction #446761

solid

Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #466871

( 2 )

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #482088

( 2 )

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #516771

( 2 )

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #518261

( 2 )

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #535094

( 2 )

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07

$C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1$

Reaction #575722

( 2 )

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12

C[C@H]1C[C@H]2O[C@@H]2CC/C=C/C(=O)Cc2c(Cl)c(O)cc(O)c2C(=O)O1

Reaction #649685

compound 2-122

Ausbeute 101.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11

Reaction #649992

8-Benzyloxy-3-methyl5-oxiranyl-1H-quinolin-2-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11

Reaction #664809

8-Benzyloxy-3-methyl-5-oxiranyl-1H-quinolin-2-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05

Reaction #743601

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12

CCCCC1OC1c1ccc(N2CC(=O)NS2(=O)=O)c(OCc2ccccc2)c1

Reaction #747895

title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12

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