Authors Murray, LAM; Fallon, T; Sumby, CJ; George, JH in AMER CHEMICAL SOC published article about STRUCTURAL ELUCIDATION; BIOMIMETIC SYNTHESIS; NAPHTHOQUINONES; MEROCHLORINS; BIOSYNTHESIS; ANTIBIOTICS in [Murray, Lauren A. M.; Fallon, Thomas; Sumby, Christopher J.; George, Jonathan H.] Univ Adelaide, Dept Chem, Adelaide, SA 5005, Australia in 2019.0, Cited 47.0. Formula: C9H10O3. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7
A concise and divergent strategy for the synthesis of the naphterpin and marinone meroterpenoid families has been developed. The approach features a succession of pericyclic reactions-an aromatic Claisen rearrangement, a retro-6 pi-electrocyclization, and two Diels-Alder reactions-which facilitated the first total synthesis of naphterpin itself in five steps from 2,5-dimethoxyphenol, alongside similar syntheses of 7-demethylnaphterpin and debromomarinone. Late-stage oxidation and bromination reactions were also investigated, leading to the first total syntheses of naphterpins B and C and isomarinone.
About 2,5-Dimethoxybenzaldehyde, If you have any questions, you can contact Murray, LAM; Fallon, T; Sumby, CJ; George, JH or concate me.. Formula: C9H10O3
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com