about
Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular ComplexityA highly reactive dicationic iridium(III) catalyst for the polarized Nazarov cyclization reactionSynthesis of (±)-tetrapetalone A-Me aglycon.Non-conventional methodologies in the synthesis of 1-indanones.Using Nazarov electrocyclization to stage chemoselective [1,2]-migrations: stereoselective synthesis of functionalized cyclopentenones.Gas-phase nazarov cyclization of protonated 2-methoxy and 2-hydroxychalcone: an example of intramolecular proton-transport catalysis.Efficient Nazarov cyclization/Wagner-Meerwein rearrangement terminated by a Cu(II)-promoted oxidation: synthesis of 4-alkylidene cyclopentenones.The role of methoxy group in the Nazarov cyclization of 1,5-bis-(2-methoxyphenyl)-1,4-pentadien-3-one in the gas phase and condensed phase.Neurotrophic natural products: chemistry and biology.Asymmetric electrocyclic reactions.Allene ether Nazarov cyclization.Assembly of functionalized carbocycles or N-heterocycles through a domino electrocyclization-[1,2] migration reaction sequence.4π electrocyclisation in domino processes: contemporary trends and synthetic applications towards natural products.Total synthesis of the Isodon diterpene sculponeatin N.Beyond the Divinyl Ketone: Innovations in the Generation and Nazarov Cyclization of Pentadienyl Cation Intermediates.Neutral Nazarov-type cyclization catalyzed by palladium(0)Asymmetric syntheses of 8-oxabicyclo[3,2,1]octane and 11-oxatricyclo[5.3.1.0]undecane from glycals.Diastereospecific nazarov cyclization of fully substituted dienones: generation of vicinal all-carbon-atom quaternary stereocenters.A mild, catalytic and efficient Nazarov cyclization mediated by phosphomolybdic acid.Rh(I)-catalyzed intramolecular [3 + 2] cycloaddition reactions of 1-ene-, 1-yne- and 1-allene-vinylcyclopropanes.Ambiphilic molecules for trapping reactive intermediates: interrupted Nazarov reaction of allenyl vinyl ketones with Me2PCH2AlMe2.Regioselective silver-mediated Kondakov-Darzens olefin acylation.On the acidity and reactivity of highly effective chiral Brønsted acid catalysts: establishment of an acidity scale.Substituent-controlled reactivity in the Nazarov cyclisation of allenyl vinyl ketones.Direct and highly diastereoselective synthesis of azaspirocycles by a dysprosium(III) triflate catalyzed aza-Piancatelli rearrangement.Recent Progress on Nazarov Cyclizations: The Use of Iron Salts as Catalysts in Ionic Liquid Solvent Systems.Nazarov reaction: current trends and recent advances in the synthesis of natural compounds and their analogs.Stereospecific Decarboxylative Nazarov Cyclization Mediated by Carbon Dioxide for the Preparation of Highly Substituted 2-Cyclopentenones.Regioselective Synthesis of α-Fluorinated Cyclopentenones by Organocatalytic Difluorocyclopropanation and Fluorine-Directed and Fluorine-Activated Nazarov Cyclization.Harnessing the Lewis Acidity of HFIP through its Cooperation with a Calcium(II) Salt: Application to the Aza-Piancatelli Reaction.The Evolution of the Total Synthesis of Rocaglamide.Lewis Acid Mediated Nazarov Cyclization as a Convergent and Enantioselective Entry to C-nor-D-homo-Steroids.The photo-Nazarov reaction: scope and application.Tandem reaction of 3-hydroxyhexa-4,5-allenic esters: a novel access to diversely substituted 2H-pyran-2-ones and indenes.One-pot relay catalysis: divergent synthesis of furo[3,4-b]indoles and cyclopenta[b]indoles from 3-(2-aminophenyl)-1,4-enynols.Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,4,9-Dienyne Esters to 3 a,6-Methanoisoindole Esters with Pro-Inflammatory Cytokine Antagonist Activity.Interrupted imino-Nazarov cyclization of 1-aminopentadienyl cation and related cascade process.1,4-Diketones from Cross-Conjugated Dienones: Potassium Permanganate-Interrupted Nazarov Reaction.Nazarov cyclization of divinyl and arylvinyl epoxides: application in the synthesis of resveratrol-based natural products.[3]Dendralene synthesis: rhodium(III)-catalyzed alkenyl C-H activation and coupling reaction with allenyl carbinol carbonate.
P2860
Q29031113-B9683DA1-2021-439F-BCC1-C0565F0C8CA6Q34546730-2CE995CE-0469-48AC-825F-51A463A2F654Q34660678-66FFA894-2722-4A5E-8DC7-6E2284BA3836Q35160884-8776485D-75DB-444C-B412-4B59382BA9ACQ36578005-7B88A4ED-D6AE-4026-98C4-3FFB2BA47FDFQ37221928-67FFD41B-064A-43A2-B766-5277ACB5D7E1Q37460427-E4C30B8A-E3F7-4E7F-9DC1-D4F6CCCA0175Q37594904-867B4354-9E44-4F41-B836-7F5C945B7BA1Q37623342-3E7C1365-747D-475D-AA74-9891F1E122F9Q37874946-86E99E6B-36A2-4451-9202-CA8CBAFEB30DQ38160321-A16CB423-2E3F-4AA9-99C0-2FFA73C10933Q38566855-5689F65A-6747-47C5-AFD8-41FB10AEBF07Q38600310-B046290A-2C0E-476A-8E4B-9F8F3D85BA90Q39024710-CDB1219D-6725-419A-A8AC-1C2983D4B74DQ41871708-F0D15423-7691-413E-8EAE-5233EB1C902AQ42066838-BAA379EF-39A9-4651-94E0-B9DD643B724FQ42285500-83C690E2-DC50-4C4F-BD6F-92985E7826A1Q42777242-35AA0E1D-5F49-4EEC-9117-A9DDD479BD22Q43176733-7ED59114-57A1-457C-B76E-494C25D2C010Q43176766-1A8A3076-3E37-4541-910F-F1636E54F81BQ45087148-07C92417-197F-4C59-A527-8A568FCEA570Q46318906-B3B06C8C-351E-4794-9795-C1476A6E8ACDQ46403444-5843A43A-DA07-4D68-B994-A46888218087Q46502028-298079AD-D96C-4F0D-8DC2-8308A2FB1070Q46656176-5A35B8BE-6074-4ACD-8EC1-D9BFC5CF4DA2Q47741030-63985113-4D57-4E39-945B-97724D7EB892Q47902517-86D9A963-49C2-4DDE-A174-29ADB4E416C5Q48094964-39C9FFED-9179-4EA5-9094-15F9B6AAA4F0Q48183416-253E9631-95F1-457D-A2F9-8788053CDE57Q48286621-8D54DD0C-D386-41B9-8A77-58AA95B8A391Q48292393-90FE33F4-1BF2-446D-829C-4A4393694E0FQ48359051-EEC3554E-CC44-4B64-9C03-A6B184FB0BFEQ50454577-B1CC74E9-C789-4647-8199-69F62CB88433Q50502276-8128DFB5-B8C0-4A77-85E6-CD97D2393F31Q50873492-7B8F5D97-4F4B-48B0-ACA2-CA2C7709B338Q50912687-2DAD93D2-3BD0-45A0-8ACE-28E8B16FECE0Q51058518-E548E6E9-E9DE-40D5-9C40-BC7308C98686Q52933376-A82811EC-AE5E-48C3-88FE-BDA17A655D57Q53582477-2E9DA4FE-92A0-467E-A446-2145DC5AE4F8Q54765621-46696A83-401B-49D7-B076-F0C96EF3D3DF
P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Recent developments in the Nazarov process
@ast
Recent developments in the Nazarov process
@en
type
label
Recent developments in the Nazarov process
@ast
Recent developments in the Nazarov process
@en
prefLabel
Recent developments in the Nazarov process
@ast
Recent developments in the Nazarov process
@en
P1433
P1476
Recent developments in the Nazarov process
@en
P2093
Hélène Pellissier
P304
P356
10.1016/J.TET.2005.04.014
P577
2005-07-01T00:00:00Z