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supporting information of alexy virgil bartberger and

supporting information of alexy virgil bartberger and

12345NextA Versatile Hexadiene Synthesis by Decarboxylative sp3sp3

Jul 20,2006·Wen-Bo Liu,Noriko Okamoto,Eric J.Alexy,Allen Y.Hong,Kristy Tran,Brian M.Stoltz,Enantioselective -Alkylation of ,-Unsaturated Malonates and Ketoesters by a Sequential Ir-Catalyzed Asymmetric Allylic Alkylation/Cope Rearrangement,Journal of the American Chemical Society,10.1021/jacs.6b02153,138,16,(5234-5237),(2016).Cited by 13Publish Year 2017Author Eric J.Alexy,Scott C.Virgil,Michael D.Bartberger,Brian M.StoltzEnantioselective Pd-Catalyzed Decarboxylative Allylic ·Substrates were enolized in generally high levels of selectivity (see supporting information for details).A variety of substrates containing different alkyl and aryl substituents were examined,with all alkylated products obtained in excellent yields (Table 2).

Cited by 16Publish Year 2015Author Ulma Cersosimo,Andrea Sgorbissa,Carmen Foti,Sara Drioli,Rosario Angelica,Andrea Tomasella,RaffEnantioselective Pd-Catalyzed Decarboxylative Allylic

Oct 06,2017·Alexy EJ(1),Virgil SC(1),Bartberger MD(2),Stoltz BM(1).Author information (1)Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering,Division of Chemistry and Chemical Engineering,California Institute ofEnantioselective Pd-Catalyzed Decarboxylative Allylic Organic Letters DOI 10.1021/acslett.7b02354Enantioselective Pd-Catalyzed Decarboxylative Allylic Supporting Information for Alexy,Virgil,Bartberger,and Stoltz SI1 Supporting Information for Enantioselective Pd-Catalyzed Decarboxylative Allylic Alkylation of Thiopyranones.Access to Acyclic,Stereogenic -Quaternary Ketones.Eric J.Alexy,a Scott C.Virgil,a Michael D.Bartberger

Iridium-Catalyzed Stereoselective Allylic Alkylation

Nov 28,2016·Sponge worthy The unique combination of crotyl chloride,lithium chloride,and proton sponge has delivered the first enantio-,diastereo-,and regioselective iridium-catalyzed allylic alkylation reaction to form an all-carbon quaternary stereocenter with an aliphatic-substituted electrophile.The reaction proceeds with good to excellent selectivity for a range of substituted tetralones Palladium-Catalyzed Decarboxylative Asymmetric Allylic Shengming Ma.In this communication,we will report a palladium-catalyzed decarboxylative allenylation of benzyl carbonates and tert-butyl carbonates of 2,3-allenol with 3-oxocarboxylic acid.The PalladiumCatalyzed Enantioselective Decarboxylative Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Protected Benzoin-Derived Enol Carbonates Rémi Lavernhe,a Eric J.Alexy,a Haiming Zhang,b and Brian M.Stoltza,* a Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering,Division of Chemistry and Chemical Engineering,California Institute of Technology,Pasadena,California 91125,United States

Supporting Information of Alexy,Virgil,Bartberger,and

Supporting Information of Alexy,Virgil,Bartberger,and Stoltz SI24 13C NMR (100 MHz,CDCl 3) of compound 2b.Infrared spectrum (Thin Film,NaCl) of compound 2b.Synthesis and Evaluation of Therefore,this study provides new mechanistic information and guidance for the development of new acridones for application in the treatment of CML.View Show abstractSynthesis,Characterization and Optimization for in Vivo To illustrate mining strategies supporting therapeutic studies,transcript expression was determined 1) relative to other models,2) with successive in vivo passage,and 3) during the in vitro to

Synthesis,Characterization,and Optimization for in Vivo

Find more information about Crossref citation counts. Supporting Information Supporting Information Get e-Alerts.Download Hi-Res Image Download to MS-PowerPoint Cite This J.Med.Chem.2015 58 4 1691 Eric J.Alexy,Scott C.Virgil,Michael D.Bartberger,and Brian M.Stoltz .

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