مشارك في 169 تفاعل

12474

C/C1=C/C[C@@H](/C(C)=C/c2csc(C)n2)OC(=O)C[C@H](O)C(C)(C)C(=O)[C@H](C)[C@@H](O)[C@@H](C)CCC1.CC(O)COC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@@H](O[C@H]7[C@H](O)[C@@H](O)[C@@H](O[C@H]8[C@H](O)[C@@H](O)[C@@H](O[C@H]1[C@H](O)[C@H]2O)O[C@@H]8COCC(C)O)O[C@@H]7COCC(C)O)O[C@@H]6COCC(C)O)O[C@@H]5COCC(C)O)O[C@@H]4COCC(C)O)O[C@@H]3COCC(C)O
Reaction #8665
Epothilone D Hydroxypropyl-β-Cyclodextrin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1c(F)cc2ncc(F)c3c2n1CC3(O)CO
Reaction #43415
solid
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1c(F)cc2ncc(F)c3c2n1CC3(O)CO
Reaction #43434
solid
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@](O)(CO)c1cc(Br)ccc1F
Reaction #67507
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cccc(CC[C@H](O)CO)c1OCc1ccccc1
Reaction #76223
(2S)-4-[2-(benzyloxy)-3-methoxyphenyl]-1,2-butanediol
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)C(=O)OCn1cc(-c2cccc(Br)c2)nn1
Reaction #157476
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCC(n2cc(COc3ccc(S(C)(=O)=O)cc3)nn2)CC1
Reaction #167831
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@@](O)(CO)c1cc(Br)ccc1F
Reaction #168754
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)C[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CCS(C)(=O)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CN)[C@@H](C)O)[C@@H](C)O)C(C)C)[C@@H](C)O)C(=O)O
Reaction #214792
H-Gly-Gly-Phe-Met(O2)-Thr-Ser-Glu-Lys-Ser-Gln-Thr-Pro-Leu-Val-Thr-Leu-OH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=C(O)c1cn(Cc2c(F)cccc2F)nn1
Reaction #305994
1-(2,6-Difluorobenzyl)-1H-1,2,3-triazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(O)c1cn(Cc2c(F)cccc2F)nn1
Reaction #305995
1-(2,6-Difluorobenzyl)-1H-1,2,3-triazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
OC[C@H](O)C1CCOCC1
Reaction #308771
(1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
C[C@@](O)(CO)c1cc(Br)ccc1F
Reaction #308907
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N1CCCC(=O)CC1
Reaction #329719
1-t-butoxycarbonyl-4-oxohomopiperidine
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[Si](C)(C)OC1(CC(O)CO)CCC1
Reaction #340320
3-(1-(tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCCCCCCCC(O)CO
Reaction #344452
decane 1,2-diol
المردود 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
C[C@@](O)(CO)CCOCc1ccccc1
Reaction #419254
compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CN(C(=O)NCc1cccc(F)c1Cl)[C@H](CO[Si](C)(C)C(C)(C)C)C[C@@H](O)CO
Reaction #428167
1-((2S,4R)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COC(=O)c1ncc(C(=O)O)c2c1OC(C)(C)OC2
Reaction #489754
8-(methoxycarbonyl)-2,2-dimethyl-4H-[1,3]dioxino[4,5-c]pyridine-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CN(C(=O)NCc1cccc(F)c1Cl)[C@H](CO[Si](C)(C)C(C)(C)C)C[C@@H](O)CO
Reaction #497029
1-((2S,4R)-1-(tert-butyldimethylsilyloxy)-4,5-dihydroxypentan-2-yl)-3-(2-chloro-3-fluorobenzyl)-1-methylurea
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
الصفحة 1التالي