112471-51-9Relevant articles and documents
Tetrahydropyranylation of alcohols and phenols catalyzed by a new polystyrene-bound tin(IV) porphyrin
Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Mohammadpoor-Baltork, Iraj,Gharaati, Shadab
, p. 95 - 101 (2011)
In the present work, tetrahydropyranylation of alcohols and phenols with 3,4-dihydro-2H-pyran (DHP) catalyzed by tetrakis(p-aminophenyl) porphyrinatotin(IV) trifluoromethanesulfonate, [SnIV(TNH 2PP)(OTf)2], supported on chloromethylated polystyrene is reported. The prepared catalyst was characterized by elemental analysis, FT-IR and diffuses reflectance UV-Vis spectroscopic methods. This new heterogenized catalyst was found as efficient and reusable catalyst for tetrahydropyranylation of primary, secondary and tertiary alcohols as well as phenols at room temperature.
Alkyl- and arylation of oxacyclic ethers with triethylsilyl triflate-2,4,6-collidine-Gilman reagent combination: Remarkable discrimination of two ether oxygens
Fujioka, Hiromichi,Ohnaka, Takuya,Okitsu, Takashi,Kubo, Ozora,Okamoto, Kazuhisa,Sawama, Yoshinari,Kita, Yasuyuki
, p. 529 - 540 (2007)
The alkylation reaction of oxacyclic ethers such as THP-ethers, THF-ethers, etc., has been developed. The treatment of oxacyclic ether with TESOTf and 2,4,6-collidine gives the collidinium salt intermediate obtained by the reaction of the cyclic oxygen at
Tetrahydropyranylation of alcohols and phenols catalyzed by a new multi-wall carbon nanotubes-bound tin(IV) porphyrin
Gharaati, Shadab,Kargar, Hadi,Falahati, Ali Mohammad
, p. 1169 - 1178 (2017)
Abstract: In the present study, tetrahydropyranylation of alcohols and phenols with 3,4-dihydro-2H-pyran (DHP) using tetrakis(p-aminophenyl)porphyrinatotin(IV) trifluoromethanesulfonate, [SnIV(TNH2PP)(OTf)2], and tetrakis(p-aminophenyl)porphyrinatotin(IV) tetrafluoroborate, [SnIV(TNH2PP)(BF4)2], supported on multi-wall carbon nanotubes as new catalytic systems is investigated. These new catalysts, [SnIV(TNH2PP)(OTf)2@MWCNT] and [SnIV(TNH2PP)(BF4)2@MWCNT], were characterized using elemental analysis, FT-IR spectroscopic techniques, scanning electron microscopy and diffuse reflectance UV–Vis spectroscopic methods. In these catalytic systems, an optimization on the amounts of catalysts and amount of DHP was done in the tetrahydropyranylation of alcohols and phenols with DHP and the best outcomes were received in the presence of 0.01?mmol (40?mg) of [SnIV(TNH2PP)(OTf)2@MWCNT] and [SnIV(TNH2PP)(BF4)2@MWCNT] with 2?mmol of DHP. Efficiency and reusability are two important features of these new heterogenized catalysts for tetrahydropyranylation of primary, secondary and tertiary alcohols as well as phenols at room temperature. These catalysts were recovered several times with no loss on their initial activity, which indicates their high reusability and stability. Graphical Abstract: In the present study, tetrahydropyranylation of alcohols and phenols with 3,4-dihydro-2H-pyran (DHP) using tetrakis(p-aminophenyl)porphyrinatotin(IV) trifluoromethanesulfonate, [SnIV(TNH2PP)(OTf)2], and tetrakis(p-aminophenyl)porphyrinatotin(IV) tetrafluoroborate, [SnIV(TNH2PP)(BF4)2], supported on multi-wall carbon nanotubes as new catalytic systems is investigated. These new catalysts, [SnIV(TNH2PP)(OTf)2@MWCNT] and [SnIV(TNH2PP)(BF4)2@MWCNT], were characterized using elemental analysis, FT-IR spectroscopic techniques, scanning electron microscopy and diffuse reflectance UV–Vis spectroscopic methods. In these catalytic systems, an optimization on the amounts of catalysts and amount of DHP was done in the tetrahydropyranylation of alcohols and phenols with DHP and the best outcomes were received in the presence of 0.01?mmol (40?mg) of [SnIV(TNH2PP)(OTf)2@MWCNT] and [SnIV(TNH2PP)(BF4)2@MWCNT] with 2?mmol of DHP. Efficiency and reusability are two important features of these new heterogenized catalysts for tetrahydropyranylation of primary, secondary and tertiary alcohols as well as phenols at room temperature. These catalysts were recovered several times with no loss on their initial activity, which indicates their high reusability and stability. [Figure not available: see fulltext.].
Practical Intermolecular Hydroarylation of Diverse Alkenes via Reductive Heck Coupling
Gurak, John A.,Engle, Keary M.
, p. 8987 - 8992 (2018/09/11)
The hydroarylation of alkenes is an attractive approach to construct carbon-carbon (C-C) bonds from abundant and structurally diverse starting materials. Herein we report a palladium-catalyzed reductive Heck hydroarylation of aliphatic and heteroatom-substituted terminal alkenes and select internal alkenes with an array of (hetero)aryl iodides. The reaction is anti-Markovnikov selective with terminal alkenes and tolerates a wide variety of functional groups on both the alkene and (hetero)aryl coupling partners. Additionally, applications of this method to complex molecule diversifications are demonstrated. Mechanistic experiments are consistent with a mechanism in which the key alkylpalladium(II) intermediate is intercepted with formate and undergoes a decarboxylation/C-H reductive elimination cascade to afford the saturated product and turn over the cycle.
BiCl3: A versatile catalyst for the tetrahydropyranylation and depyranylation of 1°,2°,3°, allylic, benzylic alcohols, and symmetric diols
Vijaya Durga,Balamurali Krishna,Baby Ramana,Santha Kumari,Vijay,Hari Babu
, p. 1030 - 1034 (2017/05/26)
Bismuth trichloride as mild reagent, has been found to be a worthful catalyst for tetrahydropyranylation of 1°,2°,3°, allylic, benzylic alcohols, and symmetric di-ols. At room temperature the reagent THP(3,4-dihydro-2H-pyran) was successfully employed as pyranylating agent in presence of BiCl3catalyst without the use of a solvent and the yields of the products were found to be 90-96%. Further, the depyranylation of alcohols was achieved in quantitative yield by simple addition of MeOH using the same catalyst. The developed method was showed good chemo-selectivity in symmetrical diols for mono THP protection.
