120686-98-8

Upstream product

• 91274-05-4 (2S,3S)-1,2-O-isopropylidene-1,2,3,4-tetrol 
• 100-39-0 benzyl bromide 
• 93367-08-9 Kalium-<4S-(R*,S*)>-α-hydroxy-2,2-dimethyl-1,3-dioxolan-4-acetat 

Downstream Products

• 114185-00-1 1,2-di-O-benzyl-L-threitol 
• 120687-00-5 <2R-(2α(S*,S*),3aα,4β,7β,7aα)>-Octahydro-7,8,8-trimethyl-2-<2,3,4-tris(phenylmethoxy)butoxy>-4,7-methanobenzofuran 
• 183888-75-7 (2S,3S)-3,4-Bis-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-butan-2-ol 
• 153096-71-0 (S)-3,4-Bis-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-butan-2-one 
• 120686-99-9 <2R-(2α(S*,S*),3aα,4β,7β,7aα)>-1-<(Octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl)oxy>-3,4-bis(phenylmethoxy)-2-butanol 

Relevant academic research and scientific papers

Synthesis of protected enantiopure erythrulose derivatives

D- and L-Erythrulose derivatives 2-6 bearing protective O-silyl and O-benzyl groups in various positions were synthesized in enantiopure form from L-ascorbic acid, D-isoascorbic acid, and D-glucose. VCH Verlagsgesellschaft mbH, 1996.

Chiral Lactols, VIII - A Way for the Asymmetric Induction in the Formation of Sugars

The substituted glycol aldehyde 4 which bears an enantiomerically pure acetal-type protective group exhibiting the configuration of an α-L-sugar at the acetal centre is subjected to aldolization under basic conditions.The resulting products are reduced and characterized by comparison with reference compounds of known absolute configuration.L-Sugars are formed preferentially with L-erythrose being the main product.