Day: October 26, 2022

Lee, Anna; Scheidt, Karl A. published an article in 2015, the title of the article was N-Heterocyclic carbene-catalyzed enantioselective annulations: a dual activation strategy for a formal [4+2] addition for dihydrocoumarins.Name: (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate And the article contains the following content:

A highly efficient asym. formal [4+2] annulation for the synthesis of dihydrocoumarins has been developed via an in situ activated NHC catalysis. Both electrophilic and nucleophilic species are generated in situ simultaneously whereby acyl imidazoles facilitated rapid formation of an NHC-enolate intermediate to afford the [4+2] dihydrocoumarin adducts. The experimental process involved the reaction of (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate(cas: 1469801-67-9).Name: (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate

The Article related to nitrogen heterocyclic carbene catalyzed enantioselective formal annulation addition, dihydrocoumarin adduct preparation in situ activated nhc catalyst, acylimidazole facilitated nhc enolate intermediate formation, in situ generated electrophile nucleophile dihydrocoumarin preparation and other aspects.Name: (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Vorona, Svetlana V.; Zevatskii, Yuri E.; Myznikov, Leonid V. published an article in 2019, the title of the article was Zinc (II) Chloride as Phase Transfer Catalyst and as Catalyst of Cycloaddition Azide Ion to Heterocumulenes and Terminal Alkynes in Organic Solvents.Name: 4-(p-Tolyl)-1H-1,2,3-triazole And the article contains the following content:

The system of NaN3-ZnCl2 in organic solvents was effective for azide ion cycloaddition to heterocumulenes and terminal alkynes. The reaction proceeded readily in the case of heterocumulenes, so these transformations fall into the category of click reactions. The study on the reaction mechanism showed that role of zinc salt consists in transferring azide ion to the organic phase and decreasing the energy barrier of nucleophilic addition of azide ion to the unsaturated substrate. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Name: 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to isothiocyanate sodium azide zinc chloride catalyst cycloaddition, thiotetrazole preparation, carbodiimide sodium azide zinc chloride catalyst cycloaddition, aminotetrazole preparation, terminal alkyne sodium azide zinc chloride catalyst regioselective cycloaddition, triazole preparation and other aspects.Name: 4-(p-Tolyl)-1H-1,2,3-triazole

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

On January 14, 2015, Goodman, C. Guy; Walker, Morgan M.; Johnson, Jeffrey S. published an article.Computed Properties of 1469801-67-9 The title of the article was Enantioconvergent Synthesis of Functionalized γ-Butyrolactones via (3 + 2)-Annulation. And the article contained the following:

A dynamic kinetic resolution of β-halo α-keto esters, RO2CC(:O)CHXR’ [R = Me, Bu-t, R’ = CH2Ph, X = Cl; R = Bu-t, R’ = Ph, Me, CH2CH2Me, CH2CCSiMe3, (CH2)3OCH2Ph; R = Bu-t, R’ = Ph, X = F] in an asym. homoenolate reaction is described. A chiral N-hetereocyclic carbene catalyzes the a3 → d3-umpolung addition of α,β-enals to racemic α-keto esters, forming γ-butyrolactones I [R1 = Ph, C6H4OMe-4, C6H4Cl-4, C6H4Me-4, C6H4Me-3, thien-2-yl, furan-2-yl, CH:CHPh-(E), CO3Et] and II [R2 = Ph, Me, CH2CH:CH2, CH2CCSiMe3, (CH2)3OCH2Ph, X = Cl; R = Ph, X = F] with three contiguous stereocenters. The addition occurs with high regio-, diastereo-, and enantiocontrol. This methodol. constitutes an intermol. DKR process to set three stereocenters during the key bond forming event. The experimental process involved the reaction of (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate(cas: 1469801-67-9).Computed Properties of 1469801-67-9

The Article related to butyrolactone gamma derivative enantioconvergent annulation synthesis, halo keto ester dynamic kinetic resolution asym homoenolate reaction, alkenal annulation halo keto ester hetereocyclic carbene catalyst, regioselective annulation halo keto ester alkenal hetereocyclic carbene catalyst and other aspects.Computed Properties of 1469801-67-9

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

On March 3, 2010, Grimster, Neil; Zhang, Li; Fokin, Valery V. published an article.Reference of 4-(p-Tolyl)-1H-1,2,3-triazole The title of the article was Synthesis and Reactivity of Rhodium(II) N-Triflyl Azavinyl Carbenes. And the article contained the following:

Highly reactive rhodium(II) N-trifluoromethylsulfonyl azavinyl carbenes are formed in situ from NH-1,2,3-triazoles, triflic anhydride, and rhodium carboxylates. They rapidly and selectively react with olefins, providing cyclopropane carboxaldehydes and 2,3-dihydropyrroles in generally excellent yields and high enantio- and diastereoselectivity. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Reference of 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to triazole triflic anhydride chiral rhodium carboxylate catalyst, rhodium azavinyl carbene triflyl derivative formation alkene cyclopropanation, cyclopropane carboxaldehyde stereoselective preparation, alkene rhodium triflyl azavinyl carbene dipolar cycloaddition, dihydropyrrole derivative regioselective preparation and other aspects.Reference of 4-(p-Tolyl)-1H-1,2,3-triazole

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

On September 21, 2018, Sun, Jun; Mou, Chengli; Wang, Zhongyao; He, Fangcheng; Wu, Jian; Chi, Yonggui Robin published an article.Quality Control of (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate The title of the article was Carbene-Catalyzed [4 + 2] Cycloadditions of Vinyl Enolate and (in Situ Generated) Imines for Enantioselective Synthesis of Quaternary α-Amino Phosphonates. And the article contained the following:

A carbene-catalyzed enantioselective addition of enals to five-membered cyclic imines is developed. The reaction gives chiral quaternary α-amino phosphonates bearing tetrasubstituted C centers with excellent enantioselectivities. The imine substrates can be generated in situ from the corresponding amines under an oxidative condition that is compatible with the carbene catalysis. Thus, a 1-pot cross-dehydrogenative-coupling (CDC) reaction between enals and amines is also realized with high enantioselectivity remaining. The method provides quick enantioselective access to amino phosphonates with potential applications in medicines and pesticides. The experimental process involved the reaction of (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate(cas: 1469801-67-9).Quality Control of (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate

The Article related to carbene catalyzed cycloaddition vinyl enolate imine, ketiminophosphonate cyclic preparation cycloaddition vinyl enolate carbene catalyst, quaternary alpha amino phosphonate preparation, crystal structure benzoisothiazolopyridinylphosphonate quaternary alpha amino phosphonate, mol structure benzoisothiazolopyridinylphosphonate quaternary alpha amino phosphonate and other aspects.Quality Control of (R)-5-Benzyl-2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics