Introduction of a new synthetic route about 1787246-78-9

In some applications, this compound(1787246-78-9)Related Products of 1787246-78-9 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Related Products of 1787246-78-9. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (5aS,10bR)-2-(2,6-Diethylphenyl)-4,5a,6,10b-tetrahydro-2H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-11-ium tetrafluoroborate, is researched, Molecular C22H24BF4N3O, CAS is 1787246-78-9, about A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. Author is Hovey, M. Todd; Cohen, Daniel T.; Walden, Daniel M.; Cheong, Paul H.-Y.; Scheidt, Karl A..

The Armillaria and Lactarius genera of fungi produce the antimicrobial and cytotoxic mellolide, protoilludane, and marasmane sesquiterpenoids. We report a unified synthetic strategy to access the protoilludane, mellolide, and marasmane families of natural products. The key features of these syntheses are (1) the organocatalytic, enantioselective construction of key chiral intermediates from a simple achiral precursor, (2) the utility of a key 1,2-cyclobutanediol intermediate to serve as a precursor to each natural product class, and (3) a direct chem. conversion of a protoilludane to a marasmane (I → II) through serendipitous ring contraction, which provides exptl. support for their proposed biosynthetic relationships.

In some applications, this compound(1787246-78-9)Related Products of 1787246-78-9 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

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