Substructure Search

CC(C)(C)CCCBr

CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(OC2CCCCC2)c2cc(Br)ccc21
Reaction #1311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1316
Compound I
DOI: 10.6084/m9.figshare.5104873.v1
CC(=S)C1CCC(C)(C)c2ccc(Br)cc21
Reaction #1317
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C(=O)O)C1C(C(Cl)(Br)C(F)(F)F)S(C)(=O)=O
Reaction #5737
2,2-dimethyl-3-[2-trifluoromethyl-2-bromo-2-chloro-1-methylsulfonylethyl]-cyclopropane carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)C(Br)CC1c1ccccc1
Reaction #40331
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](Br)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40600
36
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N=[N+]=[N-])C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40601
38
Yield 87.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C#N)(CCCBr)C(C)C)cc1OC
Reaction #50094
crude product
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(=O)CC[C@@H]12
Reaction #50340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CCCBr)(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #63587
α-(3-bromopropyl)-4-fluoro-α-(4-fluorophenyl)benzeneacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63588
intermediate 17
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63589
intermediate 18
DOI: 10.6084/m9.figshare.5104873.v1
CC12CC3(C)CC(c4cc(Br)cc(Br)c4)(C1)CC(C14CC5(C)CC(C)(CC(c6cc(Br)cc(Br)c6)(C5)C1)C4)(C2)C3
Reaction #69565
7,7′-bis(3,5-dibromophenyl)-3,3′,5,5′-tetramethyl-1,1′-biadamantane
Yield 180.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)CCCBr
Reaction #76254
5bromo-2,2-dimethyl-pentan-1-ol
Yield 100.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCCBr)COC1CCCCO1
Reaction #76255
5-bromo-1-(tetrahydropyranyloxy)-2,2-dimethylpentane
Yield 94.7%DOI: 10.6084/m9.figshare.5104873.v1
[C-]#[N+]C(CCCC(C)(C)COC1CCCCO1)(CCCC(C)(C)COC1CCCCO1)S(=O)(=O)c1ccc(C)cc1
Reaction #76256
2-[6-isocyano-2,2,10,10-tetramethyl-11-(tetrahydropyran-2-yloxy)-6-(toluene-4-sulfonyl)-undecyloxy]-tetrahydropyran
Yield 113.2%DOI: 10.6084/m9.figshare.5104873.v1
[C-]#[N+]C(CCCC(C)(C(=O)OCC)c1ccccc1)(CCCC(C)(C(=O)OCC)c1ccccc1)S(=O)(=O)c1ccc(C)cc1
Reaction #76267
2,10-dimethyl-6-isocyano-6-(4-tolyl-sulfonyl)-2,10-diphenyl-undecanedioic acid diethyl ester
Yield 117.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)(CCCBr)c1ccccc1
Reaction #76269
5-bromo-2-methyl-2-phenyl-pentan-1-ol
Yield 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCCBr)(COC1CCCCO1)c1ccccc1
Reaction #76270
2-(5-bromo-2-methyl-2-phenyl-pentyloxy)-tetrahydropyran
Yield 96.2%DOI: 10.6084/m9.figshare.5104873.v1
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