223524-30-9

Upstream product

• 340013-40-3 C₂₉H₃₂O₅ 
• 340013-27-6 (1R,4S,5R,6S)-4,5,6-Tris-benzyloxy-cyclohex-2-enol 
• 340013-57-2 (4S,5R,6R)-4,5,6-tris(benzyloxy)cyclohex-2-en-1-one 
• 85798-11-4 (4S,5R,6S)-4,5,6-tris-benzyloxycyclohex-2-en-1-one 

Downstream Products

• 340013-58-3 1-Methoxy-4-((1S,4S,5R,6S)-4,5,6-tris-benzyloxy-cyclohex-2-enyloxymethyl)-benzene 
• 103066-43-9 (3S,4R,5R)-tribenzyloxy-(6R)-hydroxycyclohexene 

Relevant academic research and scientific papers

A new convergent route to aldohexoses from a common chiral building block.

[reaction in text] A diastereocontrolled route to the eight aldohexoses has been developed starting from a common cyclohexanoid chiral building block.

INTRAMOLECULAR AMINO DELIVERY REACTIONS FOR THE SYNTHESIS OF VALIENAMINE AND ANALOGUES

Iodocyclization and sigmatropic rearrangement reactions of N-substituted carbonimidothioates are used to prepare valienamine (1), 7-norvalienamine (8), and the valienamine-based pseudo-disaccharide 12. Key words: carbonimidothioates; iodocyclization; rearrangement; glucosidase inhibitors; pseudo disaccharides