1628535-40-9

Upstream product

• 1628535-39-6 5-(bromomethyl)-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]-dioxin-4-one 
• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 940289-70-3 7-hydroxy-2,2,5-trimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 1628535-38-5 7-methoxy-2,2,5-trimethyl-4H-benzo[d][1,3]dioxin-4-one 

Downstream Products

• 1628535-34-1 7-methoxy-2,2-dimethyl-5-((1-phenyl-1H-tetrazol-5-ylsulfon-yl)-methyl)-4H-benzo[d][1,3]dioxin-4-one 
• 66018-41-5 zeaenol 

Relevant academic research and scientific papers

The protecting-group directed diastereoselective Nozaki-Hiyama-Kishi (NHK) reaction: Total synthesis and biological evaluation of zeaenol, 7-epi-zeaenol and its analogues

The stereoselective total synthesis of zeaenol and 7-epi-zeaenol is achieved in a convergent manner using Julia-Kocienski olefination, protecting group-directed intermolecular diastereoselective Nozaki-Hiyama-Kishi (NHK) reaction, De Brabander's lactoniza

Stereoselective total syntheses of paecilomycins e and F through a protecting group directed diastereoselective intermolecular Nozaki-Hiyama-Kishi (NHK) reaction

An efficient and concise approach to the total syntheses of paecilomycins E (1) and F (2) is described. A protecting group directed intermolecular diastereoselective Nozaki-Hiyama-Kishi (NHK) reaction, a Julia-Kocienski olefination, a Sharpless asymmetric dihydroxylation, and De Brabander's lactonization protocol are used as the key steps.