479669-01-7

Upstream product

• 100-39-0 benzyl bromide 
• 479669-00-6 (3aR,4aR,6S,7R,8S,8aR,8bR)-7,8-Bis-hydroxymethyl-2,2,7-trimethyl-hexahydro-benzo[4,5]furo[2,3-d][1,3]dioxole-6,8a-diol 
• 479669-05-1 (3aR,5R,6R,6aR)-5-((S)-2-Hydroxy-3-methyl-but-3-enyl)-2,2-dimethyl-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 479668-97-8 (3aR,5R,6R,6aR)-5-((R)-2-Hydroxy-3-methyl-but-3-enyl)-2,2-dimethyl-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 479668-92-3 Acetic acid (3aR,4aR,6S,7S,8R,8aR,8bR)-8-chloromethyl-8a-hydroxy-2,2,7-trimethyl-7-(2,2,2-trichloro-ethyl)-octahydro-benzo[4,5]furo[2,3-d][1,3]dioxol-6-yl ester 
• 479668-95-6 (3aR,5R,6R,6aR)-2,2-Dimethyl-5-(2-trityloxy-ethyl)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 479668-98-9 C₁₉H₂₅ClO₈ 
• 479668-93-4 C₁₈H₂₄O₉ 
• 479668-91-2 Acetic acid (S)-1-((3aR,5R,6R,6aR)-6-hydroxy-2,2-dimethyl-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl)-2-methyl-allyl ester 
• 479668-96-7 (3aR,5R,6R,6aR)-5-(2-Hydroxy-ethyl)-2,2-dimethyl-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 322390-88-5 1,2-O-Isopropylidene-6-O-triphenylmethyl-3-C-vinyl-α-D-allofuranose 

Downstream Products

• 479669-02-8 (1R,2S,3S,4R,5S)-2,5-Bis-benzyloxy-3,4-bis-benzyloxymethyl-2-hydroxymethyl-4-methyl-cyclohexanol 

Relevant academic research and scientific papers

Synthesis of the CD ring system of paclitaxel by atom-transfer radical annulation reaction

Atom-transfer radical annulation of diene derived from D-glucose under Kharasch conditions provided access to the fully functionalized CD ring system of paclitaxel.