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From Heteroaromatic Acids and Imines to Azaspirocycles: Stereoselective Synthesis and 3D Shape AnalysisThe dearomative annulation between N-2-pyridylamidine and CO2 toward pyrido[1,2-a]-1,3,5-triazin-4-ones.The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis.A reaction mode of carbene-catalysed aryl aldehyde activation and induced phenol OH functionalization.Tandem dienone photorearrangement-cycloaddition for the rapid generation of molecular complexity.Syntheses of arnottin I and arnottin II.Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade ReactionEnantioselective synthesis of hindered cyclic dialkyl ethers via catalytic oxa-Michael/Michael desymmetrization.Chiral hypervalent iodine reagents: synthesis and reactivity.Recent advances in dearomatization of heteroaromatic compounds.Synthesis of Spirocyclic Indolenines.Asymmetric transformations of achiral 2,5-cyclohexadienones.Asymmetric dearomatization of phenols.Dearomatization through Halofunctionalization Reactions.1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis.ipso-Cyclization: an emerging tool for multifunctional spirocyclohexadienones.Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones.Pd(0)-Catalyzed Dearomative Diarylation of Indoles.Unraveling the intramolecular cyclization mechanism of oxidized tryptophan in aqueous solution as a function of pH.Evolution of a short route to strychnine by using the samarium-diiodide-induced cascade cyclization as a key step.Highly Efficient Cascade Reaction for Selective Formation of Spirocyclobutenes from Dienallenes via Palladium-Catalyzed Oxidative Double Carbocyclization-Carbonylation-Alkynylation.Catalyst-Driven Scaffold Diversity: Selective Synthesis of Spirocycles, Carbazoles and Quinolines from Indolyl Ynones.Gold(I)-catalyzed dearomative Rautenstrauch rearrangement: enantioselective access to cyclopenta[b]indoles.Enantioselective total synthesis of (-)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids.Rhodium(I)-Catalyzed Benzannulation of Heteroaryl Propargylic Esters: Synthesis of Indoles and Related Heterocycles.Recent developments in the catalytic, asymmetric construction of pyrroloindolines bearing all-carbon quaternary stereocenters.Efficient syntheses of (-)-crinine and (-)-aspidospermidine, and the formal synthesis of (-)-minfiensine by enantioselective intramolecular dearomative cyclization.Hydroxyl regioisomerization of anthracycline catalyzed by a four-enzyme cascade.Enantioselective dearomatization of isoquinolines by anion-binding catalysis en route to cyclic α-aminophosphonates.Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design?Electrophilicity: the "dark-side" of indole chemistry.Palladium(0)-catalyzed intramolecular dearomative arylation of pyrroles.Cascade oxidative dearomatization/semipinacol rearrangement: an approach to 2-spirocyclo-3-oxindole derivatives.An expedient stereoselective and chemoselective synthesis of bicyclic oxazolidinones from quinols and isocyanates.Brønsted Acid-Catalyzed Tandem Cyclizations of Tryptamine-Ynamides Yielding 1H-Pyrrolo[2,3-d]carbazole Derivatives.Enantioselective Dearomatization of Naphthol Derivatives with Allylic Alcohols by Cooperative Iridium and Brønsted Acid Catalysis.Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles.Enantioselective Borylative Dearomatization of Indoles through Copper(I) Catalysis.Intermolecular enantioselective dearomatization reaction of β-naphthol using meso-aziridine: a bifunctional in situ generated magnesium catalyst.Dearomatization of electron poor six-membered N-heterocycles through [3 + 2] annulation with aminocyclopropanes.
P2860
Q28821526-03CB5B66-3AF4-4A1D-BCF1-85D67E1278B8Q33470371-B41F9EFC-DD86-41EF-BADB-50AF5FF991E5Q33797639-D0564359-A631-44D1-9499-B3E0A43F2EB1Q33815749-58C18E15-F396-480B-A969-E5260B04191EQ35026613-9CFB7FE0-7F0A-4B96-92D2-4A28A0CA53F4Q35678237-1005516C-D3A9-4AA8-BDD0-634941FD5BECQ36832301-73BC4355-C89A-472B-933E-448C96E54B5CQ37661505-EDD8C483-4A5D-4974-BA20-92AEB3931663Q38165889-082402BB-1CE7-4B7A-B7EA-EDE613045648Q38215898-D1EF3F55-2823-4839-A899-C867C37D579BQ38667646-90FA892F-A764-4715-BCB4-0F2CC6761FA4Q38674921-CD9829FA-F0A0-44B4-B45A-8FF912055A14Q38689052-7A9C8D50-5D93-48F7-9D4E-1F0203123411Q38885664-E498805F-73B0-43D0-9F0B-F671DF8ABBAEQ38989386-C3E3948F-4ED9-4E08-8489-F2476C1ABC7AQ39198551-AB831C76-F052-43F2-8DF7-AD63C1394229Q39391118-2FD9B000-EAD2-4ED3-BEF4-2D6172685E19Q39945844-4E32D0AE-A261-41BE-A176-A8802275D3A0Q40731215-CBD90B68-6D28-43A0-9F90-61D36FD28AF3Q41331386-BBD434B2-6D77-4243-90F3-8F5EC1FB343BQ41602903-27C5B98C-40F9-4C74-BC7F-E5CC4CC77B97Q41607485-707A3F6A-E16E-4C4B-B4A6-7251913C0558Q41625219-3927999C-7903-4726-B0CC-9DC095B0FEA0Q41671057-E2D5C324-38C9-4BC7-9EC0-0BA592A7115FQ41887371-53AAA8FB-D0B2-4E32-8796-17EC5111B1BDQ41898204-AB43F956-51C1-45D0-A964-75BA17BAD994Q42035737-8679B4FA-6D65-4062-85AE-23197F616555Q42084241-25B2231B-57A3-458A-B2E7-42692B2CB057Q42211369-FB775E03-4D3D-46E0-A00D-E7B615C169F9Q42796234-1ED45FEE-BBC7-45CF-8D32-47E53A30960AQ43775392-72C32F3E-4E7C-4030-8C1F-FD11A1555CE4Q44272998-BC966F3A-E94E-4AFA-ACC2-C9C2A7CB7476Q44996223-D3B878FD-C25F-4B20-808D-93CC1A4878A7Q46013312-561734BA-27E8-4C58-8E67-D79C61277D67Q46255469-875C2C86-BEF2-4814-887E-5E70E513FE53Q46418235-071437AD-51D6-421E-B941-9162C500A16AQ46520174-9E264507-9B96-4D96-A4EB-05D8FCE737D7Q46712091-40801AE7-684A-49F6-94A3-5072AA116C95Q46786520-3DD11A41-5358-432F-9435-B767D5C7DDCFQ47124388-459D2B7C-E29E-4073-9193-F93C86457D3B
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
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artículo científico
@es
name
Catalytic asymmetric dearomatization reactions.
@en
type
label
Catalytic asymmetric dearomatization reactions.
@en
prefLabel
Catalytic asymmetric dearomatization reactions.
@en
P2093
P356
P1476
Catalytic asymmetric dearomatization reactions.
@en
P2093
Chun-Xiang Zhuo
Shu-Li You
P304
12662-12686
P356
10.1002/ANIE.201204822
P407
P577
2012-12-03T00:00:00Z