بحث البنية الفرعية

1251566

C=COCCC1(O)C2CC3CC(C2)CC1C3
Reaction #50901
2-Hydroxy-2-adamantylethyl Vinyl Ether
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(c2ncc[nH]2)C23CC4CC(CC(C4)C2O)C3)cc1
Reaction #64189
4-[2-hydroxy-adamant-1-yl-1-(imidazolyl)methyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC12CC3CC(C1)C(O)C(C3)C2)OCc1ccccc1
Reaction #66731
desired product
المردود 53.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(OC(=O)COC(=O)CO)C2CC3CC(C2)CC1C3
Reaction #72403
objective compound
المردود 67.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3
Reaction #72404
compound 3
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)OC1C2CC3CC(C2)CC1C3
Reaction #83115
2-Adamantylchloroformate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@](C)(Cc1c[nH]c2ccccc12)NC(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83116
title compound
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@](Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)O
Reaction #83117
acid
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[O-]
Reaction #83122
carbonate
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1c[nH]c2ccccc12
Reaction #83127
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1csc2ccccc12
Reaction #83128
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1nc2ccccc2[nH]1
Reaction #83129
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCC1=CCCc2ccccc21
Reaction #83130
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1cccs1
Reaction #83131
product
المردود 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cccc1CCNC(=O)C(C)(Cc1c[nH]c2ccccc12)NC(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83132
Tricyclo[3.3.1.13,7 ]dec-2-yl (±)-[1-(1H-indol-3-ylmethyl)-1-methyl-2-[[2-(1-methyl-1H-pyrrol-2-yl) ethyl]amino]-2-oxoethyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1ccccn1
Reaction #83133
product
المردود 72186.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1c[nH]cn1
Reaction #83134
product
المردود 47.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1cnccn1
Reaction #83135
desired product
المردود 63.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1ccco1
Reaction #83136
desired product
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC(C)OC(=O)NC(C)(Cc1c[nH]c2ccccc12)C(=O)NCCc1ccc2ccccc2n1
Reaction #83137
product
المردود 17.1%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي