1263309-86-9

Upstream product

• 148918-17-6 1-bromo-4,5-dimethyl-2-(prop-2-en-1-yloxy)benzene 
• 22802-39-7 2-bromo-4,5-dimethylphenol 
• 95-65-8 3,4-Dimethylphenol 

Downstream Products

• 1263309-87-0 3-bromo-5, 6-dimethyl-2-hydroxybenzaldehyde 
• 1263309-88-1 2-formyl-3,4-dimethylphenyltrifluoromethanesulfonate 
• 1263309-89-2 5,6-dimethyl-2-vinylbenzaldehyde 
• 1263309-85-8 1-(2-vinyl-8, 9-dimethylphenyl)prop-2-en-1-ol 
• 42373-90-0 2-hydroxy-5,6-dimethylbenzaldehyde 

Relevant academic research and scientific papers

Stereochemistry, total synthesis, and biological evaluation of the new plant hormone solanacol

The first total synthesis of solanacol, a member of the strigolactone family, features ring-closing metathesis, enzymatic kinetic resolution, and atom-transfer radical cyclization. This defines the stereostructure of the natural product. The best hormonal

New synthesis of A-ring aromatic strigolactone analogues and their evaluation as plant hormones in pea (pisum sativum)

A new general access to A-ring aromatic strigolactones, a new class of plant hormones, has been developed. The key transformations include in sequence ring-closing metathesis, enzymatic kinetic resolution and a radical cyclization with atom transfer to install the tricyclic ABC-ring system. The activity as plant hormones for the inhibition of shoot branching in pea of various analogues synthesized by this strategy is reported. Inhibiting shoot branching: A new general access to A-ring aromatic strigolactones (see scheme), a new class of plant hormones, has been developed. The biological activity of various analogues synthesized by this strategy for inhibiting bud outgrowth in pea was evaluated. Copyright