153442-02-5

Upstream product

• 153442-03-6 C₂₃H₂₀N₄O₁₂ 

Downstream Products

• 153442-04-7 (R)-3-[(R)-1,2-Bis-(tert-butyl-dimethyl-silanyloxy)-ethyl]-3-methyl-cyclohexene 
• 153442-06-9 (3R,4R)-4-[(R)-1,2-Bis-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-1-trimethylsilanyloxy-3-vinyl-cyclohexene 
• 153442-07-0 (2S,3R,4R)-4-[(R)-1,2-Bis-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-hydroxymethyl-4-methyl-3-vinyl-cyclohexanone 
• 153442-05-8 (R)-4-[(R)-1,2-Bis-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-methyl-cyclohex-2-enone 

Relevant academic research and scientific papers

A Concise Synthesis of Enantiomerically Pure Taxane C-Ring via the Wittig Rearrangement

An efficient, stereoselective synthesis of an enantiomerically pure C-ring precursor 14-S of O-cinnamoyltaxicins-I and -II has been achieved from 3-methyl-2-cyclohexen-1-ol, using a Wittig rearrangement as the key step.