about
The pentadehydro-Diels-Alder reactionRates of hexadehydro-Diels-Alder (HDDA) cyclizations: impact of the linker structure.Mechanism of the reactions of alcohols with o-benzynes.Rearrangement reactions of 1,1-divinyl-2-phenylcyclopropanes.Competition between classical and hexadehydro-Diels-Alder (HDDA) reactions of HDDA triynes with furan.Triple Aryne-Tetrazine Reaction Enabling Rapid Access to a New Class of Polyaromatic HeterocyclesReactions of HDDA-Derived Benzynes with Sulfides: Mechanism, Modes, and Three-Component Reactions.Synthesis of biaryls using aryne intermediates.Aryne multifunctionalization with benzdiyne and benztriyne equivalents.Analyzing Reaction Rates with the Distortion/Interaction-Activation Strain Model.The Phenol-Ene Reaction: Biaryl Synthesis via Trapping Reactions between HDDA-Generated Benzynes and Phenolics.The hexadehydro-Diels-Alder reaction: a new chapter in aryne chemistry.Construction of Condensed Polycyclic Aromatic Frameworks through Intramolecular Cycloaddition Reactions Involving Arynes Bearing an Internal Alkyne Moiety.On-surface generation and imaging of arynes by atomic force microscopy.Reductive Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or Phosphorescent Rhodium 2,2'-Biphenyl Complexes.Hexadehydro-Diels-Alder (HDDA)-Enabled Carbazolyne Chemistry: Single Step, de Novo Construction of the Pyranocarbazole Core of Alkaloids of the Murraya koenigii (Curry Tree) Family.Cyclization of Ynamide-Tethered 1,3,8-Triynes.Convenient and highly efficient routes to 2 H-chromene and 4-chromanone derivatives: iodine-promoted and p-toluenesulfonic acid catalyzed cascade cyclizations of propynols.
P2860
Q28833635-16A20B25-6F86-48D6-8FB0-D7251309E889Q34141804-C9D0D517-2751-4399-94E5-3AC9BB296BAFQ34282744-0E4215C5-9204-4F5F-9103-243ED13A4A4BQ35006054-CD35BAD9-6422-4619-9EE7-422523610757Q35647211-062EE6F9-AE2B-49BC-85EB-829B50EA6BE3Q36062131-3277A754-7D0B-4ED5-A40B-20422A182AD8Q37471063-F185FD9D-3377-4310-926F-8F578392B5B6Q38983509-C547FDE9-5B90-47C2-B454-6136B3D8DAE3Q39144371-2F97164D-ABBD-451E-98E9-67113B5ACBE5Q39266241-433B904C-2126-48A8-B311-DEC2B718A478Q42742728-849BFE3B-4950-464E-A9A6-2D805B39047BQ43110829-6CF59FD9-E805-4CD3-A22F-8018F3CD3FAFQ47663991-7B907F21-DCED-48A0-91AC-7FBD4BC46312Q48155610-611C4E71-DBF5-4906-8029-FB6397118C28Q48182018-6AD82774-03A4-47A9-904B-C889A33F3378Q50750704-E5C9336C-16DF-4670-BD7D-B64D98B8D2B2Q50907058-80701749-940C-449E-8927-0D0A6E127802Q51017755-57C4DD50-BD80-4E6A-8B28-093ED06C5D9A
P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
The aromatic ene reaction
@ast
The aromatic ene reaction
@en
The aromatic ene reaction
@nl
type
label
The aromatic ene reaction
@ast
The aromatic ene reaction
@en
The aromatic ene reaction
@nl
prefLabel
The aromatic ene reaction
@ast
The aromatic ene reaction
@en
The aromatic ene reaction
@nl
P2860
P356
P1433
P1476
The aromatic ene reaction
@en
P2093
Thomas R Hoye
P2860
P2888
P356
10.1038/NCHEM.1797
P50
P577
2013-11-17T00:00:00Z
P5875
P6179
1046630051