부분 구조 검색

CCO.Cc1ccccc1

CCCCO[PH](=O)Cc1ccccc1
Reaction #1638
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOP(=O)(CO)Cc1ccccc1
Reaction #1639
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1ccccc1)N=Cc1ccccc1
Reaction #6020
N-benzylidene-D-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H](O)Cc1ccccc1
Reaction #11018
(2S)-2-hydroxy-3-phenylpropionic acid
수율 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(C(Cc2ccc(F)cc2)C(=O)O)CC1
Reaction #40645
69NLS56
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)CCNC(=O)OCc1ccccc1
Reaction #45692
Benzyl [2-(dimethylcarbamoyl)ethyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)CCCNC(=O)OCc1ccccc1
Reaction #45702
solid
수율 82.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49376
4-[2-(dimethylamino)ethoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCON1Cc2cccc(-c3cc4cc(CN5CCCCC5)ccc4n3C(=O)OC(C)(C)C)c2C1=O
Reaction #49377
(3-(tert-butoxycarbonylamino)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OCCCO[Si](C)(C)C(C)(C)C)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49378
4-[3-(tert-butyldimethylsilyloxy)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 53.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCOc1ccc(-c2cc3cc(C=O)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49399
4-[3-(tert-butoxycarbonylamino)propoxy]-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone
수율 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OCc3ccccc3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49402
4-benzyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCCOc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49403
4-(2-isopropoxyethoxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCOc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49404
4-[3-(dimethylamino)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CCCOc2ccc(-c3cc4cc(CN5CCCCC5)ccc4n3C(=O)OC(C)(C)C)c3c2CNC3=O)CC1
Reaction #49405
4-[3-(4-methylpiperazin-1-yl)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cc(OCCCO[Si](C)(C)C(C)(C)C)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49592
4-chloro-5-[3-(tert-butyldimethylsiloxy)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
수율 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCO)OCc1ccccc1
Reaction #50193
title compound ( b )
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCOC(=O)c1ccccc1)OCc1ccccc1
Reaction #50194
title compound ( c )
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CC(=O)NC(C)C(=O)OCC(C)C)cc1
Reaction #51347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CC(=O)N[C@@H](C)C(=O)OCC(C)C)cc1
Reaction #51385
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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