بحث البنية الفرعية

B(F)(F)F

CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC1C=CC(=O)C1
Reaction #2643
title compound
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(C(c3c4c(c(C(=O)OC)c5c3OC(C)(C)O5)OC(C)(C)O4)c3c4c(c(C(=O)OC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2695
Bis-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis (1,3) dioxol-4-yl)-mono-(8-methoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiol-4-yl) methane
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncoc1C(C)(N=[N+]=[N-])c1ccoc1
Reaction #2931
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](NC(=O)OCc1ccc(OC)cc1)C(=O)OCc1ccccc1
Reaction #3873
title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2ccc(C)nc2c1O
Reaction #4884
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(O)ccc2ncccc12
Reaction #4886
6-Hydroxy-5-quinolinecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCC1=C(C(=O)O)N2C(=O)C(N)[C@H]2SC1
Reaction #5254
3-allyloxymethyl-7-amino-ceph-3-eme-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCOCC1=C(C(=O)O)N2C(=O)C(N)[C@H]2SC1
Reaction #5255
3-propoxymethyl-7-amino-ceph-3-eme-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OCC1=C(C(=O)O)N2C(=O)C(N)[C@H]2SC1
Reaction #5256
3-isopropoxymethyl-7-amino-ceph-3-eme-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC1C(=O)N2C(C(=O)O)=C(OCc3ccccc3)CS[C@H]12
Reaction #5257
3-benzyloxy-7-amino-ceph-3-eme-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)C1Cc2c(Br)ccc(OC)c2C1=O
Reaction #5446
white solid
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCCCCCC(C(=O)OCC)NC1=O
Reaction #5490
ethyl 3-methylidene-2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(CBr)cc(CBr)cc1CBr
Reaction #5648
nitro
المردود 86.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cccc2cnccc12)N1Cc2cc(O)c(O)cc2CC1CN1CCN(c2ccccc2)CC1
Reaction #5816
title compound
المردود 90.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(C#N)cc1
Reaction #6128
expected product
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(C(C)=O)cc1
Reaction #6133
expected product
المردود 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C[S+](Cc2ccc(Cl)cc2)c2ccc(Cl)cc2)cc1.F[B-](F)(F)F
Reaction #6384
4-chlorophenylbis(4-chlorobenzyl)sulfonium tetrafluoroborate
المردود 77.4%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CC2SCCCS2)cc1
Reaction #6482
title compound
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C)c(F)c1
Reaction #7001
3-fluoro-4-methyl anisole
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي