Поиск подструктуры

9073

O=C(NCC#Cc1cn([C@H]2CC[C@@H](CO)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #4985
alkynylamino nucleoside
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC1CCCP(=O)(Oc2ccccc2)O1
Reaction #6432
2-phenoxy-2-oxo-6-(azidomethyl)-1,2-oxaphosphorinane
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CI)CN(Cc2ccccc2)C(C(=O)OCc2ccccc2)CO1
Reaction #40467
4-benzyl-6-iodomethyl-6-methyl-morpholine-3-carboxylic acid benzyl ester
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(Cc2ccccc2)C(C(=O)OCc2ccccc2)CO1
Reaction #40468
4-benzyl-6,6-dimethyl-morpholine-3-carboxylic acid benzyl ester
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
ICCOc1ccc(Cc2ccc(-c3ncco3)cc2)cc1
Reaction #44787
2-[4-[[4-(2-iodoethoxy)phenyl]methyl]phenyl]oxazole
Выход 78.5%DOI: 10.6084/m9.figshare.5104873.v1
c1coc(-c2ccc(Cc3ccc(OCCNCCN4CCOCC4)cc3)cc2)n1
Reaction #44809
N-[2-[4-[[4-(2-oxazolyl)phenyl]methyl]phenoxy]ethyl]-4-morpholineethanamine
Выход 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)COC(CI)(c1ccccc1)c1ccccc1
Reaction #48672
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(c2ccccc2)(c2ccccc2)OC[C@@H]1COCc1ccccc1
Reaction #48673
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCC(CC1(C(=O)O)CCCC1)C(=O)OC(C)(C)C
Reaction #51187
crude title compound
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c1c3cc(F)ccc3[nH]c1c1c2c2cc(F)ccc2n1[C@@H]1O[C@H](CI)C[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #52144
3,9-difluoro-12-(2,3-di-O-benzyl-4,6-dideoxy-6-iodo-β-D-glucopyranosyl)-6,7,12,13-tetrahydro(5H)indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7-dione
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(I)ccc(OC(C)=O)c1F
Reaction #52341
title compound
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc2[nH]ccc2c1
Reaction #69340
5-(2-methoxyethoxy)-1H-indole
Выход 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(I)ccc(OC(C)=O)c1F
Reaction #79906
title compound
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(C(OCCI)=C2C3CC4CC(C3)CC2C4)c1
Reaction #81039
product
Выход 102.9%DOI: 10.6084/m9.figshare.5104873.v1
NCCOC(=C1C2CC3CC(C2)CC1C3)c1cccc(O)c1
Reaction #81040
product
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #82178
5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #82180
5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid methyl ester
Выход 62.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #82181
ketorolac methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(I)CCn1cccc1C(=O)c1ccccc1
Reaction #82182
4-(2-benzoylpyrrol-1-yl)-2-iodobutyric acid methyl ester
Выход 91.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[C@H]1O[C@@H](n2cc(C)c(=O)[nH]c2=O)C[C@@H]1O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #82914
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее