About: 6-exo-trig Michael addition-lactonizations for catalytic enantioselective chromenone synthesis

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About: 6-exo-trig Michael addition-lactonizations for catalytic enantioselective chromenone synthesis Goto Sponge NotDistinct Permalink

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scientific article published on 30 January 2017

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2017 (ast) наукова стаття, опублікована в січні 2017 (uk) scientific article published on 30 January 2017 (en) مقالة علمية نشرت في 30 يناير 2017 (ar)
publication date	wds:Q37711821-E78BEC72-02C7-47D9-9869-A336BEAC0386
publication date	2017-01-30 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37711821-D5788987-144F-4FF7-8CF8-12CF6A55FA79
language of work or name	English
cites work	wds:Q37711821-06EB0E38-7B33-4E82-957A-F9E4D490C641 wds:Q37711821-0D4A715A-F7F1-4A21-83F2-67E049B36811 wds:Q37711821-123B1189-E8C5-41A3-B626-4FFF6A9B3935 wds:Q37711821-15344631-1597-4FB3-B42B-34193F0ECEBE wds:Q37711821-161CCE26-DE62-43C1-BF8F-9CFEB8E8B13F wds:Q37711821-224C0950-EEF7-4E44-BCEB-D946CC39C503 wds:Q37711821-28448FBB-4DCE-4A43-BE5D-3A35FB9C4C65 wds:Q37711821-28E65612-9834-4EBA-9513-8214F2EFA18F wds:Q37711821-28ED6E91-A7A8-4505-ABAF-A792210989D3 wds:Q37711821-29FDC726-3398-49AD-8607-A9FA8DF47FCF wds:Q37711821-2D102FC4-A150-43AB-9BBA-CFC3D4B75206 wds:Q37711821-31AD0173-36BB-45EF-8C92-165628A8E62C wds:Q37711821-3E5B9B0E-E4DB-4D0B-B663-B372A1CA0862 wds:Q37711821-4D65060B-505B-46AB-ACD0-097FC3BC8039 wds:Q37711821-58E327A5-0977-4EF6-8413-98983C17D3F0 wds:Q37711821-5AA8FE0C-3A44-48E4-A60D-18E24380C8D4 wds:Q37711821-5DCD8060-7372-4035-92C4-08A8F0AB7FDD wds:Q37711821-61EBC8B9-08FA-412F-A4B7-18D86EE60123 wds:Q37711821-62D25949-FE54-4F8D-854A-A07DE8711A56 wds:Q37711821-66438F78-934E-4CB0-9DAD-097A8D8B3858 wds:Q37711821-7080A756-EEEF-4A8C-A768-77666F5D0149 wds:Q37711821-712B91FB-2F3D-43C5-8641-7EB81E87E99B wds:Q37711821-7E20F5DA-9AB1-44EF-BFBB-4A4F64738FA2 wds:Q37711821-876343DA-42F5-4E69-9694-D6C5D0C42128 wds:Q37711821-8A505591-A6E2-4D5D-BCB6-CA0778C45986 wds:Q37711821-8AF18D91-B9DC-4EF7-8160-305CA0F3905D wds:Q37711821-8D076506-E926-4B42-99F2-C944F2488568 wds:Q37711821-923E3179-8073-4E23-855E-717B8731AAF3 wds:Q37711821-9471301A-611D-41EF-9CF9-F4BEB0B331FA wds:Q37711821-9E9E899B-1EEC-446C-B014-2DFD57BB9EB1 wds:Q37711821-A2E79989-7175-4869-A72B-A3F62E6B4201 wds:Q37711821-A4EFBE97-F8FC-4078-B813-9E9A8C6768C4 wds:Q37711821-A7E1D0C6-E436-45F2-AAE3-65E85E48AF39 wds:Q37711821-AE96D5FC-A210-49C3-89F2-B0DD2708DB8B wds:Q37711821-C01D6C80-BDBD-4179-A34D-15E9A5880988 wds:Q37711821-DE062791-2A0A-4F28-B1F6-5052FEF97D9A wds:Q37711821-E9FF821D-B3B5-41A5-81CC-C1F52ED57EFD wds:Q37711821-FB364F31-9F5C-425C-8D7B-4103E5B904AD
cites work	Concise total synthesis of (+/-)-salinosporamide A, (+/-)-cinnabaramide A, and derivatives via a bis-cyclization process: implications for a biosynthetic pathway? Copper-catalyzed C-H functionalization reactions: efficient synthesis of heterocycles Bicyclic- and tricyclic-beta-lactones via organonucleophile-promoted bis-cyclizations of keto acids: Enantioselective synthesis of (+)-dihydroplakevulin Chiral heterocycles by iminium ion cyclization Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles Transition-metal-catalyzed reactions in heterocyclic synthesis Benzotetramisole: A Remarkably Enantioselective Acyl Transfer Catalyst Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation A Survey of the Role of Noncovalent Sulfur Interactions in Drug Design. Stereoelectronic effects dictate molecular conformation and biological function of heterocyclic amides. Stereodivergent organocatalytic intramolecular Michael addition/lactonization for the asymmetric synthesis of substituted dihydrobenzofurans and tetrahydrofurans. Recent developments in the use of catalytic asymmetric ammonium enolates in chemical synthesis Silver-mediated synthesis of heterocycles. Isothiourea-catalysed enantioselective pyrrolizine synthesis: synthetic and computational studies. Amidines, isothioureas, and guanidines as nucleophilic catalysts. Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates. Acylammonium salts as dienophiles in Diels-Alder/lactonization organocascades. Intermolecular Sulfur···Oxygen Interactions: Theoretical and Statistical Investigations Effects of Methyl Substituents on the Activity and Enantioselectivity of Homobenzotetramisole-Based Catalysts in the Kinetic Resolution of Alcohols Alkyl C-O ring cleavage of bicyclic beta-lactones with Normant reagents: synthesis of a Merck IND intermediate. Origin of Enantioselectivity in Benzotetramisole-Catalyzed Dynamic Kinetic Resolution of Azlactones Isothiourea-Catalyzed Enantioselective Carboxy Group Transfer Telescoped Synthesis of Stereodefined Pyrrolidines Nonaromatic amidine derivatives as acylation catalysts Highly stereoselective asymmetric Pummerer reactions that incorporate intermolecular and intramolecular nonbonded S...O interactions Organocatalytic functionalization of carboxylic acids: isothiourea-catalyzed asymmetric intra- and intermolecular Michael addition--lactonizations Synthesis of heterocycles via electrophilic cyclization of alkynes containing heteroatom Total synthesis of (+)-omphadiol Dyotropic rearrangements of fused tricyclic β-lactones: application to the synthesis of (-)-curcumanolide A and (-)-curcumalactone Natural and synthetic chromenes, fused chromenes, and versatility of dihydrobenzo[h]chromenes in organic synthesis Silanediol-Catalyzed Chromenone Functionalization Enantioselective copper-catalyzed 1,3-dipolar cycloadditions Homobenzotetramisole: an effective catalyst for kinetic resolution of aryl-cycloalkanols A C(2)-symmetric chiral bis-sulfoxide ligand in a rhodium-catalyzed reaction: asymmetric 1,4-addition of sodium tetraarylborates to chromenones Asymmetric synthesis of bicyclic beta-lactones via the intramolecular, nucleophile-catalyzed aldol lactonization: improved efficiency and expanded scope Intramolecular, nucleophile-catalyzed aldol-lactonization (NCAL) reactions: catalytic, asymmetric synthesis of bicyclic beta-lactones Bioinspired total synthesis and human proteasome inhibitory activity of (-)-salinosporamide A, (-)-homosalinosporamide A, and derivatives obtained via organonucleophile promoted bis-cyclizations Double diastereoselective, nucleophile-catalyzed aldol lactonizations (NCAL) leading to beta-lactone fused carbocycles and extensions to beta-lactone fused tetrahydrofurans
author name string	wds:Q37711821-8DE16974-30C7-4CCB-BCB4-DDCF6A9EE63C
author name string	Rifahath M Neyyappadath
rdfs:label	6-exo-trig Michael addition-lactonizations for catalytic enantioselective chromenone synthesis (en)

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