224433-58-3

Upstream product

• 100-39-0 benzyl bromide 
• 103066-43-9 (3S,4R,5R)-tribenzyloxy-(6R)-hydroxycyclohexene 
• 195873-70-2 (3R,4R,5R,6S)-3,4,5,6-tetra(benzoyloxy)-1,7-octadiene 
• 50-70-4 D-sorbitol 
• 277744-76-0 2,3,4,5-tetra-O-benzyl-D-gluco-hexodialdose 
• 256342-72-0 2,3,4,5-tetrakis-benzyloxyhexane-1,6-diol 
• 277744-69-1 1,6-di-O-[(4-methoxyphenyl)-diphenylmethyl]-D-glucitol 
• 277744-72-6 1,6-di-O-[(4-methoxyphenyl)-diphenylmethyl]-2,3,4,5-tetra-O-benzyl-D-glucitol 
• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 
• 195873-66-6 (3S,4R,5R)-tribenzyloxy-(6R)-hydroxyocta-1,7-diene 
• 195873-65-5 (2S,3R,4S)-2,3,4-Tris-benzyloxy-hex-5-enal 
• 1023310-53-3 2,3,4,5-tetra-O-benzyl-1,6-di-O-trityl-D-glucitol 
• 29780-95-8 1,6-di-O-trityl-D-glucitol 
• 195873-64-4 3,4,5-tri-O-benzyl-1,2-dideoxy-D-xylohept-1-enitol 

Downstream Products

• 13035-64-8 3,4,5,6-tetra-O-benzyl-L-chiro-inositol 

Relevant academic research and scientific papers

Enantio- and diastereodivergent synthetic route to multifarious cyclitols from D-xylose via ring-closing metathesis

Short stereoselective syntheses of various cyclitols, including the derivatives of conduritol B, conduritol F, myo-inositol, and chiro-inositol have been accomplished. The key steps in the syntheses are a ring-closing metathesis process and a diastereodiv

Ruthenium carbene complexes with imidazol-2-ylidene ligands: Syntheses of conduritol derivatives reveals superior RCM activity

Syntheses of conduritol A, E and F derivatives are described using galactitol, D-mannitol and D-glucitol, respectively, as the starting materials. The key steps of this approach comprise a Tebbe olefination reaction for the preparation of dienes 15, 21 and 27 followed by ring closing metathesis (RCM) for the formation of the polyhydroxylated cyclohexene rings of the targets. A comparative study shows that the latter transformation is best achieved with catalytic amounts of ruthenium carbene complex 3a bearing one PCy3 and one 2,3-dihydro-1H-imidazol-2-ylidene ligand in its coordination sphere. (C) 2000 Elsevier Science Ltd.

A straightforward synthesis of perbenzylated conduritols from alditols by ring closing olefin metathesis

The synthesis of perbenzylated conduritols A, E and F has been achieved in six steps by formal conversion of galactitol, D-mannitol and D-glucitol into the respective terminal dienes, followed by ring closing olefin metathesis. The Royal Society of Chemistry 1999.

Synthesis of cyclitols via ring-closing metathesis

A convenient synthesis of enantiomerically pure and differentially protected L-chiro- and myo-inositols as well as conduritols B and F from 2,3,4-tri-O-benzyl-D-xylopyranose via ring-closing metathesis is reported. The facile synthesis of conduritol B con