Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
about
Methodology for the Construction of the Bicyclo[4.3.0]nonane CoreDesign, synthesis, and biological evaluation of a biyouyanagin compound librarySynthesis of cortistatins A, J, K and L.Total synthesis of (±)-cortistatin J from furan.A hypervalent iodine-induced double annulation enables a concise synthesis of the pentacyclic core structure of the cortistatins.Asymmetric synthesis of dihydroindanes by convergent alkoxide-directed metallacycle-mediated bond formation.Synthetic studies toward (+)-cortistatin AConstructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.Towards a general diastereoselective route to oxabicyclo[3.2.1]octanes via a gold-catalysed cascade reactionThe Chemistry and Biology of Nakiterpiosin - C-nor-D-Homosteroids.Synthesis of the tetracyclic core of Illicium sesquiterpenes using an organocatalyzed asymmetric Robinson annulation.2-Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications.Recent developments in the field of oxa-Michael reactions.Hypervalent iodine reagents in the total synthesis of natural products.Synthesis of the Cortistatin Pentacyclic Core by Alkoxide-Directed Metallacycle-Mediated Annulative Cross-Coupling.Trends in applying C-H oxidation to the total synthesis of natural products.Natural product analogues: towards a blueprint for analogue-focused synthesis.Creation of readily accessible and orally active analogue of cortistatin a.Cortistatin A is a high-affinity ligand of protein kinases ROCK, CDK8, and CDK11.Formal total synthesis of (±)-cortistatin AScalable synthesis of cortistatin A and related structures.Advances in the chemistry of oxaziridines.Improved synthesis of 8-oxabicyclo[3.2.1]octanes via tandem C-H oxidation/oxa-[3,3] Cope rearrangement/aldol cyclization.Asymmetric Total Synthesis of Propindilactone G, Part 2: Enantioselective Construction of the Fully Functionalized BCDE Ring System.The asymmetric total synthesis of (+)-N-acetyl norloline.A practical deca-gram scale ring expansion of (R)-(−)-carvone to (R)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1
P2860
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P2860
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
description
2009 nî lūn-bûn
@nan
2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
@ast
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
@en
type
label
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
@ast
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
@en
prefLabel
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
@ast
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
@en
P2093
P356
P1476
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof
@en
P2093
Chek Shik Lim
Damien Polet
David Y-K Chen
K C Nicolaou
Ya-Ping Sun
P304
10587-10597
P356
10.1021/JA902939T
P407
P577
2009-08-01T00:00:00Z