402475-59-6

Upstream product

• 162239-08-9 3,4,5,7-tetra-O-benzyl-1,2-dideoxy-D-galacto-hept-1-enitol 
• 158570-84-4 2,3,4,6-tetra-O-benzyl-D-galactitol 
• 1376554-75-4 (2S,3R,4R,5R)-3,4,5-tris(benzyloxy)-2-(benzyloxymethyl)tetrahydro-2H-thiopyran 
• 1376554-96-9 (2R,3R,4S,5R,6S)-2-chloro-3,4,5-tris(benzyloxy)-6-benzyloxymethyltetrahydrothiopyran 1,1-dioxide 
• 441771-42-2 2,3,4,6-tetra-O-benzyl-1,5-di-O-mesyl-D-galactitol 
• 1357078-60-4 C₁₄H₂₂O₄ 
• 1357078-51-3 C₁₃H₂₂O₅ 
• 1357078-50-2 C₂₉H₄₀O₅Si 
• 1357078-48-8 C₂₆H₃₆O₅Si 
• 821793-31-1 C₂₈H₃₈O₆Si 
• 6386-24-9 2,3,4,6-tetra-O-benzyl-D-galactopyranose 
• 176540-14-0 3,4,5,7-tetra-O-benzyl-1,2,6-trideoxy-D-galacto-hept-1-en-6-one 
• 402475-58-5 ((3S,4R,5S)-2-methylhept-6-ene-1,3,4,5-tetrayl)tetrakis(oxy)tetrakis(methylene)tetrabenzene 

Downstream Products

• 156407-85-1 (+)-neplanocin A 

Relevant academic research and scientific papers

Total synthesis of carbocyclic nucleoside (+)-neplanocin A

Asymmetric total synthesis of (+)-neplanocin A was concisely achieved from readily available d-galactose via the regioselective and diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate and intramolecular olefin meta

Divergent synthesis of aminocyclopentitol analogues via stereoselective amination of cyclic polybenzyl ether with chlorosulfonyl isocyanate

Abstract The divergent synthesis of some novel aminocyclopentitol analogues was concisely achieved from readily available d-galactose via the highly diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate, diastereosel

Convenient one-pot synthesis of thiosugars and their efficient conversion to polyoxygenated cycloalkenes

A convenient synthesis of polyoxygenated tetrahydrothiopyrans and thiepanes from various alditol derivatives with xylo, ribo, manno, gluco, galacto, and fuco configurations is described. The preparation started from the corresponding partially protected a

Baylis-Hillman reaction based flexible strategy for the synthesis of gabosine I, gabosine G, epi-gabosine i and carba l-pentose

A combination of diastereoselective Baylis-Hillman reaction and RCM reaction set is used as the flexible strategy for the ready access to cyclohexenoid and cyclopentenoid skeletons.

Synthesis of L-cyclopentenyl nucleosides using ring-closing metathesis and palladium-mediated allylic alkylation methodologies

The enantiomeric synthesis of l-cyclopentenyl nucleosides is described. The key intermediate (+)-cyclopentenyl alcohol (8) was prepared from methyl-α-d-galactopyranoside 1 using a ring closing metathesis reaction. Transformation of the allylic alcohol 8 i

Enantioselective synthesis of carba-L-furanose precursors of carbanucleosides, using ring-closing metathesis

Carba-L-sugars were synthesized in seven steps from known tetra-O-benzyl-D-galactopyranose (3). The synthesis of cyclopentene ring has been accomplished via a ring-closing metathesis step. Schrock's catalyst was employed on the unique diene, key intermedi