Поиск подструктуры

320955

O=C(N[C@@H](Cc1ccccc1)C(=O)O)C(CS)CS
Reaction #75213
N-[2-(Mercaptomethyl)-3-mercaptopropanoyl]-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)O)C(CS)CS
Reaction #75419
N-[2-(Mercaptomethyl)-3-mercaptopropanoyl]-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)N[C@@H](CC2CCCC2)C(=O)[C@@]2(C)CO2)cc1
Reaction #87086
(2S,3R)-N-((S)-3-cyclopentyl-1-((R)-2-methyloxiran-2-yl)-1-oxopropan-2-yl)-3-hydroxy-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanamide
Выход 61.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)C(C(OC)OC)[C@H]1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(Br)ccc2F)CO1
Reaction #155608
product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(Br)ccc3F)CO2)cn1
Reaction #155609
(4aR,6R,8aS)-8a-(5-bromo-2-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@@H]1CC[C@@H](Nc2ccc(F)cc2)[C@]2(O)CCCO[C@H]12
Reaction #160827
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC(O)CC(CC(=O)NCc3ccccc3)O[Si](C)(C)C(C)(C)C)C21
Reaction #177844
DOI: 10.1039/C8SC04228D
CC(C=CC=O)C1(C)CCC(C(O[SiH](c2ccccc2)c2ccccc2)C(C)(C)C)C1(C)C
Reaction #188991
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1ccccc1)C(=O)O)C(CS)CS
Reaction #190253
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC(C(O[SiH](C)C)C(C)(C)C)CN=C1OC
Reaction #194442
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(=O)C(CC(C)C)C(=O)OCC
Reaction #194446
DOI: 10.1039/C8SC04228D
CC(C)(O)CCC(CC(O)C(Cc1cccc(F)c1)NC(=O)c1cnc2ccccc2n1)C(N)=O
Reaction #194915
DOI: 10.1039/C8SC04228D
CCc1oc(-c2ccc(C(F)(F)F)cc2)nc1COCC1CCCC(COC(C)(C)C(=O)OC(C)(C)C)C1
Reaction #196328
DOI: 10.1039/C8SC04228D
CCC(C)(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC3CC(O)CC(=O)O3)C21
Reaction #203193
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC2(CCC2)CCC1=O
Reaction #206775
DOI: 10.1039/C8SC04228D
CCOC(=O)C(F)(F)C(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #210818
DOI: 10.1039/C8SC04228D
CCC(Oc1ccc(Br)cc1)C(=O)OC1CC(C(C)(C)C)C=C2C=CC(C)C(CCC3CC(C(C)(C)C)C(O[SiH](C)C)C(=O)O3)(O[SiH](C)C)C21
Reaction #211947
DOI: 10.1039/C8SC04228D
CC(C)OC(OC(C)C)C(C)(C)C(=O)C(C)C(OC(=O)OCC(Cl)(Cl)Cl)C(C)COCc1ccccc1
Reaction #218797
32a
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(COCc1ccccc1)C(OC(=O)OCC(Cl)(Cl)Cl)C(C)C(=O)C(C)(C)C=O
Reaction #218798
67
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(OC(C)C)C(C)(C)C(=O)C(C)C(OC(=O)OCC(Cl)(Cl)Cl)C(C)COCc1ccccc1
Reaction #218802
desired product
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее