668994-35-2

Upstream product

• 181303-65-1 (3S,4S)-N-benzyl-4,5-O-isopropylidene-4,5-dihydroxypent-1-en-3-amine 
• 100777-91-1 (2S)-2,3-O-isopropylideneglyceraldehyde N-benzylimine 
• 915374-99-1 Benzyl-[(S)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-(tetrahydro-pyran-2-yloxy)-but-2-ynyl]-amine 
• 915375-01-8 Benzyl-[(Z)-(S)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-(tetrahydro-pyran-2-yloxy)-but-2-enyl]-amine 
• 915375-03-0 (S,Z)-4-(benzylamino)-4-((S)-2',2'-dimethyl-1',3'-dioxolan-4'-yl)but-2-en-1-ol 
• 668994-33-0 Allyl-benzyl-[(S)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-allyl]-amine 

Downstream Products

• 114976-76-0 1,4-dideoxy-1,4-imino-D-mannitol hydrochloride 
• 668994-37-4 (2S,3S,4R)-1-Benzyl-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pyrrolidine-3,4-diol 

Relevant academic research and scientific papers

Asymmetric synthesis of 1-benzyl-2-((S)-2′,2′-dimethyl-1′,3′-dioxolan-4′-yl)-1H-pyrrole using chiral imines

A new synthesis of chiral alkyl pyrroles and pyrrolines has been achieved in an easy straightforward way, using the addition of organometallics to chiral imines.

Efficient stereodivergent synthesis of 1,4-dideoxy-1,4-iminohexitols from an (S)-glyceraldimine

A stereodivergent synthesis of 1,4-dideoxy-1,4-imino-D-mannitol I and D-allitol III from an (S)-glyceraldimine, which is easily prepared from D-mannitol, has been achieved with overall yields of 62% and 49%, respectively. The synthesis is based on the add