Detalhe da pesquisa
1.
Rongalite-Mediated Transition Metal- and Hydride-Free Chemoselective Reduction of α-Keto Esters and α-Keto Amides.
J Org Chem
; 87(15): 9915-9925, 2022 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35839148
2.
N-Oxide-Induced Ugi Reaction: A Rapid Access to Quinoline-C2-amino Amides via Deoxygenative C(sp2)-H Functionalization.
J Org Chem
; 87(15): 10435-10440, 2022 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35849086
3.
Transition metal-free functionalization of 2-oxindoles via sequential aldol and reductive aldol reactions using rongalite as a C1 reagent.
Org Biomol Chem
; 20(24): 4926-4932, 2022 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35506377
4.
Rongalite-induced transition-metal and hydride-free reductive aldol reaction: a rapid access to 3,3'-disubstituted oxindoles and its mechanistic studies.
Org Biomol Chem
; 20(4): 808-816, 2022 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34994750
5.
Toll-like receptor-8 agonistic activities in C2, C4, and C8 modified thiazolo[4,5-c]quinolines.
Org Biomol Chem
; 11(7): 1179-98, 2013 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-23314908
6.
Reduction of amine N-oxides by diboron reagents.
J Org Chem
; 76(19): 7842-8, 2011 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21812467
7.
Synthesis of (-)-deoxoprosophylline, (+)-2-epi-deoxoprosopinine, and (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids from D-glycals.
J Org Chem
; 75(13): 4608-11, 2010 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20524655
8.
Syntheses of Human TLR8-Specific Small-Molecule Agonists.
Methods Mol Biol
; 1494: 29-44, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-27718184
9.
Structure-based design of novel human Toll-like receptor 8 agonists.
ChemMedChem
; 9(4): 719-23, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24474703
10.
Exquisite selectivity for human toll-like receptor 8 in substituted furo[2,3-c]quinolines.
J Med Chem
; 56(17): 6871-85, 2013 Sep 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-23899291
11.
Two-step, one-pot synthesis of inosine, guanosine, and 2'-deoxyguanosine O6-ethers via intermediate O6-(benzotriazol-1-yl) derivatives.
Curr Protoc Nucleic Acid Chem
; Chapter 1: Unit1.26, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22700333
12.
One-pot etherification of purine nucleosides and pyrimidines.
Org Lett
; 12(20): 4478-81, 2010 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20845979