156276-65-2

Upstream product

• 98-54-4 para-tert-butylphenol 
• 37002-45-2 (4S,5S)-2,2-dimethyl-4,5-bis(p-toluenesulfonyloxymethyl)-1,3-dioxolan 

Downstream Products

• 156276-57-2 C₄₇H₆₀O₉ 
• 188399-42-0 3-Benzyloxy-5-[(4S,5S)-5-(4-tert-butyl-phenoxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-phenol 
• 156276-61-8 Toluene-4-sulfonic acid (4S,5S)-5-{3,5-bis-[(4S,5S)-5-(4-tert-butyl-phenoxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-phenoxymethyl}-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester 
• 156276-60-7 3,5-Bis-[(4S,5S)-5-(4-tert-butyl-phenoxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-phenol 
• 188399-45-3 3-[(4S,5S)-5-(4-tert-Butyl-phenoxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-5-[(4R,5R)-5-(4-tert-butyl-phenoxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-phenol 
• 178034-66-7 C₅₄H₇₂O₁₄S 
• 188399-44-2 C₄₇H₆₀O₉ 

Relevant academic research and scientific papers

Synthesis and Structure-Optical Rotation Relationships of Homochiral, Monodisperse, Tartaric Acid-based Dendrimers

Optically active, homochiral dendrimers of both the zeroth generation 1 and first generation 2 have been synthesized from (2R,3R)-tartaric acid and phloroglucinol by an iterative, convergent method.These chiral dendrimers comprise 4-tert-butylphenoxy as t