18391-53-2

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 3006-56-2 1L-1,2:3,4-di-O-isopropylidene-5-O-methyl-6-O-p-tolylsulfonyl-chiro-inositol 
• 58769-23-6 1L-3,4,:5,6-di-O-isopropylidene-2-O-methyl-chiro-inositol 
• 6763-52-6 1L-1-O-(p-tolylsulfonyl)-chiro-inositol 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 80177-96-4 1L-5,6-O-Isopropyliden-1-O-tosyl-chiro-inosit 
• 6090-98-8 (1R,2R,3R,4S)-5-cyclohexene-1,2,3,4-tetrol 
• 76139-17-8 1D-(1N,2,4/3)-1-Azido-2,3,4-tris(benzyloxy)-5-cyclohexen 
• 3006-57-3 1L-3,4:5,6-Di-O-isopropyliden-1,2-di-O-tosyl-chiro-inosit 

Relevant academic research and scientific papers

Cyclitol Reactions, IV. Synthesis of Enantiomeric Conduritols and Amino-Conduritols

The key-intermediate for all syntheses described in this paper is the 1-O-tosylate 7 of quebrachitol (1).This leads, via 8, to the 1L-conduritol B (5) and, via 13, to the 1L-conduritol F (17).Selective displacement of the equatorial tosyloxy group in comp