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1111898

CON(C)C(=O)[C@H]1CC[C@H](NC(=O)OC(C)(C)C)CC1
Reaction #53853
trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester
収率 103.0%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H]1CC[C@H](N(C)C(=O)OC(C)(C)C)CC1
Reaction #53854
trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #53855
12.83
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1CCC(NC(=O)OC(C)(C)C)CC1
Reaction #58036
[4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCC(C=O)CC1
Reaction #58037
(4-formyl-cyclohexyl)-carbamic acid tert-butyl ester
収率 105.8%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H]1CC[C@@H](NC(=O)OC(C)(C)C)CC1
Reaction #605810
tert-butyl cis-4-(methoxy(methyl)carbamoyl)cyclohexylcarbamate
収率 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1CC[C@@H](NC(=O)OC(C)(C)C)CC1
Reaction #605811
tert-butyl cis-4-acetylcyclohexylcarbamate
収率 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCC(C=O)CC1
Reaction #911541
DOI: 10.1039/C8SC04228D
CON(C)C(=O)C1CCC(NC(=O)OC(C)(C)C)CC1
Reaction #986242
[4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCC(C=O)CC1
Reaction #986243
(4-formyl-cyclohexyl)-carbamic acid tert-butyl ester
収率 105.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCC(C(=O)c2nc3ccccc3s2)CC1
Reaction #1100094
[4-(benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester
収率 82.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CS5)CC3)nc12
Reaction #1100097
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)OCCO5)CC3)nc12
Reaction #1100098
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)OCCO5)CC3)nc2c1
Reaction #1100099
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)sc2c1
Reaction #1100100
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)OCCO5)CC3)sc2c1
Reaction #1100101
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CS5)CC3)nc12
Reaction #1100102
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)NC(=O)CO5)CC3)nc12
Reaction #1100103
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4ccc5c(c4)OCCO5)CC3)nc12
Reaction #1100104
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2sc(C(=O)[C@H]3CC[C@H](NCc4nc5ccccc5s4)CC3)nc12
Reaction #1100105
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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