Substructure Search

418728

CCCCCCCCSc1ccc(C(=O)NNC(=O)C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)cc1C(F)(F)F
Reaction #179418
DOI: 10.1039/C8SC04228D
CCCCCCCCOc1ccc(C(=O)NNC(=O)C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)cc1C(F)(F)F
Reaction #182734
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(CNc2ccccc2)COC1(C)C
Reaction #254561
DOI: 10.1039/C8SC04228D
CCCCCCCCOc1ccc(C(=O)CNC(=O)C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)cc1C(F)(F)F
Reaction #257158
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)NCC(=O)c1ccc(OCCCCCCc2ccccc2)c(C(F)(F)F)c1
Reaction #291919
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)NCC(=O)c1ccc(O)c(C(F)(F)F)c1
Reaction #302310
DOI: 10.1039/C8SC04228D
COC(=O)C1(C)COC(C)(C)N1C(=O)OC(C)(C)C
Reaction #314743
4
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)O
Reaction #314744
5
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(C)(CNc2ccccc2)COC1(C)C
Reaction #688031
(RS)-2,2,4-trimethyl-4-phenylaminomethyl-oxazolidine-3-carboxylic acid tert-butyl ester
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)NCC(=O)c1ccc(OCCCCCc2ccc(C(F)(F)F)cc2)c(C(F)(F)F)c1
Reaction #765064
DOI: 10.1039/C8SC04228D
CCCCCCCCOc1ccc(C(=O)CNC(=O)C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)cc1C(F)(F)F
Reaction #901766
DOI: 10.1039/C8SC04228D
Cc1nnc(C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)o1
Reaction #1010669
tert-butyl 2,2,4-trimethyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)-1,3-oxazolidine-3-carboxylate
Yield 27.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)s1
Reaction #1010673
tert-butyl 2,2,4-trimethyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)-1,3-oxazolidine-3-carboxylate
Yield 95.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)n1
Reaction #1010674
tert-butyl 2,2,4-trimethyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)-1,3-oxazolidine-3-carboxylate
Yield 79.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(C)(C)OC[C@@]1(C)C#N
Reaction #1010690
tert-butyl (4R)-4-cyano-2,2,4-trimethyl-1,3-oxazolidine-3-carboxylate
Yield 80.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NNC(=O)[C@]1(C)COC(C)(C)N1C(=O)OC(C)(C)C
Reaction #1010694
tert-butyl (4S)-4-[(2-acetylhydrazino)carbonyl]-2,2,4-trimethyl-1,3-oxazolidine-3-carboxylate
Yield 91.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc([C@]2(C)COC(C)(C)N2C(=O)OC(C)(C)C)s1
Reaction #1010696
tert-butyl (4S)-2,2,4-trimethyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)-1,3-oxazolidine-3-carboxylate
Yield 110.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc(C(=O)NNC(=O)C2(C)COC(C)(C)N2C(=O)OC(C)(C)C)cc1C(F)(F)F
Reaction #1049335
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(C)OC[C@]1(C)C=C(Br)Br
Reaction #1150646
crude title compound
Yield 71.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)NNC(=O)c1ccc(O)c(C(F)(F)F)c1
Reaction #1227620
DOI: 10.1039/C8SC04228D
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