Simple exploration of (E)-2-Methylbut-2-enoic acid

COA of Formula: C5H8O2. About (E)-2-Methylbut-2-enoic acid, If you have any questions, you can contact Yin, JY; Landward, MB; Rainier, JD or concate me.

An article Photoelectrocyclization Reactions of Amidonaphthoquinones WOS:000526405900031 published article about BIOSYNTHESIS; RIFAMYCIN; ALKALOIDS; CLOSURE in [Yin, Jinya; Landward, Michael B.; Rainier, Jon D.] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA in 2020, Cited 31. COA of Formula: C5H8O2. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1

Readily available acrylamide naphthoquinones can be converted into the corresponding aza-anthraquinones using 6 pi-photoelectrocyclization reactions. Not only do these reactions not proceed thermally but, as demonstrated here, they can also be used to generate a range of aza-anthraquinone and aza-tetracycline derivatives including the natural products griffithazanone A and marcanine A. Several of the aza-anthraquinones generated in this work showed antibacterial activity.

COA of Formula: C5H8O2. About (E)-2-Methylbut-2-enoic acid, If you have any questions, you can contact Yin, JY; Landward, MB; Rainier, JD or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles