Substructure Search

323551

COC(=O)C(CCCCCCCI)C(=O)OC(C)(C)C
Reaction #5510
t-butyl methyl 7-iodoheptylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C(=O)OC)CC(CCOCc2ccccc2)CCC1=O
Reaction #9361
5-(2-benzyloxy-ethyl)-1-ethyl-2-oxo-cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(CCOCc2ccccc2)CCC1=O
Reaction #9390
5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCC(C(=O)c2ccc(Br)cc2)C1
Reaction #9659
3-(4-bromo-benzoyl)-cyclohexanecarboxylic acid methyl ester
Yield 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CNc1ccc(OC(F)(F)F)cc1)NC(=O)[C@H](CCC1CCCCC1)CC(=O)N1CCOCC1
Reaction #43557
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC2CCCC(C1)C2=O
Reaction #44497
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC2CCCC(C1)C2N
Reaction #44498
9-Amino-bicyclo[3.3.1]nonane-3-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCCCCCI)C(=O)OC(C)(C)C
Reaction #50265
t-butyl methyl 7-iodoheptylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C(=O)OC)CC(CCOCc2ccccc2)CCC1=O
Reaction #57002
5-(2-benzyloxy-ethyl)-1-ethyl-2-oxo-cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(CCOCc2ccccc2)CCC1=O
Reaction #57031
5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57106
lactone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@H](CC(CC(=O)O)C(=O)OC(C)(C)C)CC1
Reaction #58041
trans-2-(4-tert-Butoxycarbonylamino-cyclohexylmethyl)-succinic acid 1-tert-butyl ester
Yield 110.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCC(C(=O)c2ccc(Br)cc2)C1
Reaction #59156
3-(4-bromo-benzoyl)-cyclohexanecarboxylic acid methyl ester
Yield 95.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=C1CCOC1=O
Reaction #65054
3-Pentylidene-dihydro-2(3H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1C/C(=C\c2ccccc2)C(=O)O1
Reaction #65056
(E)-3-(phenylmethylene)-5-butyldihydro-2 (3H)-furanone
Yield 64.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(Cc2cc(C(C)(C)C)cc(C(C)(C)C)c2)CCCCC1=O
Reaction #65912
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(c2cccc(F)c2)CCC(=O)CC1
Reaction #73463
desired material
Yield 69.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CCC2CC=CC=C2N1C(=O)C(F)(F)F
Reaction #80816
2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CO)CCC2CC=CC=C2N1
Reaction #80817
2-hydroxymethyl-2-methyltetrahydroquinoline
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC2CCCC(C1)C2O
Reaction #159321
methyl 9-hydroxybicyclo-[3.3.1]nonane-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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