55:37-Using the Suzuki Reaction in Organic Synthesis

Optimizing Organic Reactions with Design of Experiments and Principal Component Analysis

Mechanism of the Suzuki Coupling

Analogues of 3-aryl-8-isobutyl-5,6,7-trihydroxy-2-methyl-4H-chromen-4-one were synthesized with high yields via the Suzuki coupling reaction of 3-iodo-8-isobutyl-5,6,7-trimethoxy-2-methyl-4H-chromen-4-one with different aryl boronic acids.

TY - JOUR. T1 - Efficient synthesis of isoflavone analogues via a Suzuki coupling reaction. AU - Ding,Ke. AU - Wang,Shaomeng. PY - 2005/5/23. Y1 - 2005/5/23

Grignard Reaction - Organic Chemistry Portal

N2 - Analogues of 3-aryl-8-isobutyl-5,6,7-trihydroxy-2-methyl-4H-chromen-4-one were synthesized with high yields via the Suzuki coupling reaction of 3-iodo-8-isobutyl-5,6,7-trimethoxy-2-methyl-4H-chromen-4-one with different aryl boronic acids.

AB - Analogues of 3-aryl-8-isobutyl-5,6,7-trihydroxy-2-methyl-4H-chromen-4-one were synthesized with high yields via the Suzuki coupling reaction of 3-iodo-8-isobutyl-5,6,7-trimethoxy-2-methyl-4H-chromen-4-one with different aryl boronic acids.