32445-72-0

Upstream product

• 32445-71-9 2,5-Anhydro-1-O-tosyl-L-iditol 
• 98-59-9 p-toluenesulfonyl chloride 
• 28218-55-5 2,5-anhydro-L-iditol 
• 27826-73-9 2,5-anhydro-D-glucitol 
• 22144-41-8 2,5-anhydro-1,6-di-O-benzoyl-D-glucitol 
• 65729-86-4 1,3,4,6-tetra-O-acetyl-2,5-anhydro-D-glucitol 
• 117757-03-6 2,5-Anhydro-L-idose 
• 15354-69-5 5,6-anhydro-1,2-O-isopropylidene-α-D-glucofuranose 
• 80599-64-0 1,3:4,6-di-O-isopropylidene-2,5-anhydro-L-iditol 

Downstream Products

• 22474-44-8 2,5:3,6-dianhydro-1-deoxy-4-O-p-tolylsulfonyl-D-glucitol 
• 88777-14-4 2,5:3,6-dianhydro-1-O-p-tolylsulfonyl-D-glucitol 
• 84447-06-3 3,4-di-O-acetyl-2,5-anhydro-1,6-di-O-p-tolylsulfonyl-D-glucitol 
• 106193-17-3 3,4-Di-O-acetyl-2,5-anhydro-1-O-methyl-6-O-(p-tosyl)-L-iditol 
• 106193-00-4 3,4-Di-O-acetyl-2,5-anhydro-1-chlor-1-desoxy-6-O-(p-tosyl)-L-iditol 
• 106192-95-4 4-O-Acetyl-1,3:2,5-dianhydro-6-O-(p-tosyl)-L-iditol 
• 106193-09-3 2,5-Anhydro-1-O-methyl-6-O-(p-tosyl)-L-iditol 
• 106192-99-8 2,5-Anhydro-1-chlor-1-desoxy-6-O-(p-tosyl)-L-iditol 
• 86883-37-6 1,3:2,5:4,6-trianhydro-L-iditol 
• 106192-94-3 1,3:2,5-Dianhydro-6-O-(p-tosyl)-L-iditol 
• 106248-69-5 2,5-Anhydro-3,4-di-O-mesyl-1,6-di-O-(p-tosyl)-L-iditol 
• 106192-93-2 3,4-Di-O-acetyl-2,5-anhydro-1,6-di-O-(p-tosyl)-L-iditol 

Relevant academic research and scientific papers

Chiral diphosphorus compounds and their transition metal complexes

The present invention relates to chiral diphosphorus compounds and their transition metal complexes, to a process for preparing chiral diphosphorus compounds and their transition metal complexes and also to their use in asymmetric syntheses.

Chiral diphosphorus compounds and transition metal complexes thereof

Tetrahydrofuran bisphosphines of formula (I), are new. Tetrahydrofuran bisphosphines of formula (I): X1, X2 = bonds or O; R1, R2 = H, 1-20C alkyl, 1-20C fluoroalkyl, 2-20C alkenyl, 4-24C aryl, 5-25C aralkyl, 6-26C aralkenyl, NR7R8, OR8, AOR8, ANR7R8 or OC

C2-symmetric diphosphinite ligands derived from carbohydrates. The strong influence of remote stereocenters on asymmetric rhodium-catalyzed hydrogenation.

Modular ligands of C(2) symmetry (13a-e, 14a,b,d, and ent-9), systematically modified at positions 2 and 5, were easily prepared from d-glucosamine, D-glucitol, and tartaric acid, respectively. The application of these ligands in the rhodium-catalyzed hyd

SYNTHESIS OF "DOUBLE-HEADED" BIS-HOMONUCLEOSIDE ANALOGS

The synthesis of "double-headed" bis-homonucleoside analogs, containing an oxolane ring with D-arabo and L-lyxo configuration is described.As starting material differently substituted 1,6-diazido-1,6-dideoxy-2,5-anhydro-D-glucitol and L-iditol derivatives

SYNTHESIS OF 6-AMINO-2,5-ANHYDRO-6-DEOXY-AND -1,6-DIDEOXY-D-GLUCITOL AND SOME DERIVATIVES THEREOF

6-Amino-2,5-anhydro-6-deoxy- and -1,6-dideoxy-D-glucitol (44), as well as some of their derivatives, were synthesized, starting from D-mannitol. 3,4-Di-O-allyl-1,2:5,6-dianhydro-D-mannitol was converted into the 2,5-anhydro-6-bromo compound 8, the bromine

1,3:2,5:4,6-TRIANHYDRO-L-IDITOL, EIN CHIRALES 2,5,8-TRIOXATRICYCLO3,6>NONAN

The title compound 8 which represents the second known example of a trianhydride in the hexitol series is prepared in five steps from D-glucitol(=D-sorbitol).