An article Bronsted Acid Promoted Regioselective C-3 Arylation and Heteroarylation of Spiro-epoxyoxindoles for the Construction of All Carbon Quaternary Centres: A Detailed Study WOS:000458273900010 published article about FRIEDEL-CRAFTS ALKYLATION; CATALYTIC ENANTIOSELECTIVE SYNTHESIS; KINETIC RESOLUTION; MIXED 3,3′-BISINDOLES; ASYMMETRIC-SYNTHESIS; STEREOGENIC CENTERS; EFFICIENT SYNTHESIS; ORGANIC-REACTIONS; ACYCLIC SYSTEMS; LEWIS-ACID in [Hajra, Saumen; Maity, Subrata; Roy, Sayan; Maity, Ramkrishna; Samanta, Srikrishna] Sanjay Gandhi Postgrad Inst, Ctr Biomed Res, Med Sci Campus,Raebareli Rd, Lucknow 226014, Uttar Pradesh, India; [Maity, Subrata] Indian Inst Technol Kharagpur, Dept Chem, Kharagpur 721302, W Bengal, India in 2019, Cited 81. Recommanded Product: 151-10-0. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0
An efficient strategy for the synthesis of all carbon quaternary centres has been developed via Bronsted acid-promoted highly regioselective intermolecular Friedel-Crafts reactions of heteroarenes or arenes with spiro-epoxyoxindoles. In addition, we have successfully performed the ring opening reaction in relatively cheap condition using water as a solvent. Beneficially, we have utilized the methodology as the key step for the synthesis of advanced precursors of various natural and unnatural indole alkaloids.
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Reference:
Isothiazole – Wikipedia,
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