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CC1(OO1)C

Cc1c(C2CO2)c(OCc2ccc(F)cc2F)c(Br)c(=O)n1-c1c(F)cccc1F
Reaction #196117
DOI: 10.1039/C8SC04228D
OCC1(n2ncnn2)CC(COCc2ccccc2)O1
Reaction #256242
DOI: 10.1039/C8SC04228D
Cc1cc2c(C3CO3)ccc(OCc3ccccc3)c2[nH]c1=O
Reaction #331952
8-Benzyloxy-3-methyl-5-oxiranyl-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
CCCCCCCCCCCC(=O)OC1CC(c2ccccc2)N(O)C(c2ccccc2)C1
Reaction #344858
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC1CC(c2ccccc2)N(O)C(c2ccccc2)C1C
Reaction #344860
title compound
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC1C(C)C(c2ccccc2)N(O)C(c2ccccc2)C1C
Reaction #344862
title compound
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)NC1C(C)C(c2ccccc2)N(O)C(c2ccccc2)C1C
Reaction #344864
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ON(Cc1ccccc1)Cc1ccccc1
Reaction #446761
solid
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
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.v1
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.v1
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.v1
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.v1
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.v1
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.v1
Cc1cc2c(C3CO3)ccc(OCc3ccccc3)c2[nH]c1=O
Reaction #649992
8-Benzyloxy-3-methyl5-oxiranyl-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(C3CO3)ccc(OCc3ccccc3)c2[nH]c1=O
Reaction #664809
8-Benzyloxy-3-methyl-5-oxiranyl-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=CC(=O)Cn1c(=O)n(-c2ccccn2)c2ccccc21
Reaction #743601
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1OC1c1ccc(N2CC(=O)NS2(=O)=O)c(OCc2ccccc2)c1
Reaction #747895
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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