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131646

CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #94595
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #351186
trans-4-(aminomethyl)-cyclohexane carboxylic acid benzyl ester para-toluenesulfonate salt
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCCC(=O)OCc1ccccc1)NC12CC3CC(CC(C3)C1)C2
Reaction #491383
6-(3-Adamantan-1-yl-ureido)-hexanoic acid benzyl ester
Выход 180.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCCC(=O)OCc1ccccc1)NC12CC3CC(CC(C3)C1)C2
Reaction #651155
6-(3-Adamantan-1-yl-ureido)-hexanoic acid benzyl ester
Выход 180.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #667971
product
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #703590
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #926147
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #927043
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #948751
trans-4- (aminomethyl)-cyclohexane carboxylic acid benzyl ester para-toluenesulfonate salt
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #950586
product
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCNC(C(=O)OCc2ccccc2)C1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #954087
benzyl 4-methyl-2-piperidinecarboxylate p-toluenesulfonate
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #1090348
product
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.NC[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #1153926
product
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.N[C@@H]1CCC[C@H](C(=O)OCc2ccccc2)C1
Reaction #1173900
cis-3-Aminocyclohexanecarboxylic acid benzyl ester para-toluene sulphonate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCCC(=O)OCc1ccccc1)NC12CC3CC(CC(C3)C1)C2
Reaction #1264018
6-(3-Adamantan-1-yl-ureido)-hexanoic acid benzyl ester
Выход 180.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN(CC(=O)O)CC(=O)NCCCCCC(=O)OCc1ccccc1
Reaction #1575435
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.Cc1ccc(S(=O)(=O)O)cc1.NCCCC[C@H](N)C(=O)OCc1ccccc1
Reaction #1581681
L-lysine benzyl ester di-p-toluene sulfonic acid salt
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCCC(=O)OCc1ccccc1)NC12CC3CC(CC(C3)C1)C2
Reaction #1602580
6-(3-Adamantan-1-yl-ureido)-hexanoic acid benzyl ester
Выход 180.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.N[C@@H]1CCC[C@H](C(=O)OCc2ccccc2)C1
Reaction #1700666
cis-3-Aminocyclohexanecarboxylic acid benzyl ester para-toluene sulphonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1
Reaction #1806368
title compound
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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