109034-37-9Relevant academic research and scientific papers
One-pot synthesis of [6-5-6] tricyclic products via a double Diels-Alder/Nazarov tandem reaction of unsymmetrically substituted cross-conjugated diynones
Carmichael, Rachael A.,Chalifoux, Wesley A.
, p. 4084 - 4092 (2017)
A highly concise one-pot method towards biologically pertinent compounds having a [6-5-6] tricyclic framework has been established. The multicomponent reaction utilizes a tandem, double Diels-Alder cycloaddition followed by a Nazarov reaction to furnish the [6-5-6] backbone. This method produces three fused rings evolving from the construction of five new carbon-carbon bonds, a quaternary carbon, and stereogenic centers in a one-pot reaction. The products are produced with excellent regio- and diastereocontrol.
Enantioselective Synthesis of Bicyclopentane-Containing Alcohols via Asymmetric Transfer Hydrogenation
Vyas, Vijyesh K.,Clarkson, Guy J.,Wills, Martin
, p. 3179 - 3183 (2021/05/04)
Compounds a containing bicyclo[1.1.1]pentane (BCP) adjacent to a chiral center can be prepared with high enantiomeric excess through asymmetric transfer hydrogenation (ATH) of adjacent ketones. In the reduction step, the BCP occupies the position distant from the η6-arene of the catalyst. The reduction was applied to the synthesis of a BCP analogue of the antihistamine drug neobenodine.
Terminal acetylenic iminium salts – Synthesis and reactivity
Keim, Michael,Kratzer, Philipp,Derksen, Helena,Isakov, Dajana,Maas, Gerhard
, p. 826 - 844 (2019/01/04)
Various types of terminal acetylenic iminium triflates (propyne iminium salts) featuring a ketiminium or an aldimin-ium group have been prepared for the first time by protiodesil-ylation of the corresponding trimethylsilyl-substituted acetylenic iminium s
Alkyne migration in alkylidene carbenoid species: A new method of polyyne synthesis
Eisler, Sara,Chahal, Navjot,McDonald, Robert,Tykwinski, Rik R.
, p. 2542 - 2550 (2007/10/03)
The synthesis of conjugated polyyne structures via a modification of the Fritsch-Buttenberg-Wiechell (FBW) rearrangement is reported. Our adaptation provides for the 1,2-migration of an alkyne in a carbene/carbenoid intermediate that is conveniently effec
Syntheses of 4H-thiopyran-4-one 1,1-dioxides as precursors to sulfone-containing analogues of tetracyanoquinodimethane
Rule,Detty,Kaeding,Sinicropi
, p. 1665 - 1673 (2007/10/02)
Synthetic routes to the unsubstituted 4H-thiopynan-4-one 1,1-dioxide (5a), 2,6-dialkyl-substituted, 2-aryl- or 2-heteroaryl-6-alkyl-substituted, 2,6-diaryl- or diheteroaryl-substituted, and 2-heteroaryl-6-aryl-substituted 4H-thiopyran-4-one 1,1-dioxides 5b-s are described. Sodium hydrosulfide hydrate in buffered aqueous alcohol can be used as a substitute for hydrogen sulfide gas for the introduction of sulfur to methyl acrylate, to 1,5-disubstituted-1,4-pentadien-3-ones 13, or to 1,5-disubstituted-1,4-pentadiyn-3-ones 17. The double dehydrogenation of 2,3,5,6-tetrahydrothiopyran-4-one 1,1-dioxides 13 with iodine-DMSO-sulfuric acid gives thiopyran-4-one 1,1-dioxides 5 in good yield and small amounts of 1,4-pentadien-3-ones 13. 2,3,5,6-Tetrahydrothiopyran-4-one 1,1-dioxide (9) and 5,6-dihydrothiopyran-4-one 1,1-dioxide (12), which lack aryl or heteroaryl substituents, give poor yields of 4H-thiopyran-4-one 1,1-dioxide (5a) with iodine-DMSO-sulfuric acid.
2. Tetraethynylethenes: Fully Cross-Conjugated ?-Electron Chromophores and Molecular Scaffolds for All-Carbon Networks and Carbon-Rich Nanomaterials
Anthony, John,Boldi Armen M.,Rubin, Ives,Hobi, Markus,Gramlich, Volker,et al.
, p. 13 - 45 (2007/10/02)
The preparation of tetraethynylethene (3,4-diethynylhex-3-ene-1,5-diyne) 1 as well as of a great diversity of differentially mono-, di-, and triprotected derivatives by newly developed synthetic routes is described.These fully cross-conjugated molecules a
Preparation of Arylpropiolate Esters from Trichlorocyclopropenium Cation and Elaboration of the Esters to Unsymmetrical 1,4-Pentadiyn-3-ones and Unsymmetrical Tellurapyranones
Wadsworth, Donald H.,Geer, Susan M.,Detty, Michael R.
, p. 3662 - 3668 (2007/10/02)
The addition of aromatic compounds including thiophene, naphthalene derivatives, and some benzene derivatives to trichlorocyclopropenium cation gave nearly quantitative yields of 1-aryl-2,3,3-trichlorocyclopropenes.Alcoholysis of the cyclopropene derivatives gave either arylpropiolate esters or arylpropiolate orthoesters (in the presence of added amine base).The arylpropiolates can be converted to unsymmetrical 1,4-pentadiyn-3-ones by two different approaches.The first approach involved reduction of the arylpropiolate esters with diisobutylaluminum hydride to give the corresponding propargyl alcohol.Pyridinium chlorochromate or manganese dioxide oxidation of the alcohol gave the propargyl aldehydes.Addition of a lithium acetylenide gave a 1,4-pentadiyn-3-ol, which could then be oxidized to the 1,4-pentadiyn-3-one with 10percent chromic acid or manganese dioxide.The second pathway used a Lewis acid mediated coupling of a propargylic acid chloride with a (trimethylsilyl)acetylene to give the 1,4-pentadiyn-3-ones directly.The coupling of 2-thiophenepropiolic acid chloride gave the product of HCl addition to the expected 1,4-diynone.The regiochemistry of addition was determined to be chloride addition to the thiophene-bearing triple bond on the basis of 1H NMR studies.The diynones were converted to unsymmetrical 2,6-disubstituted tellura-4H-pyran-4-ones with disodium telluride anion.
