905280-16-2

Upstream product

• 78008-36-3 (R)-2,3-cyclohexylideneglyceraldehyde 
• 226546-07-2 (Z)-((4-bromobut-2-en-1-yl)oxy)(tert-butyl)diphenylsilane 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 87770-83-0 (Z)-4-((tert-butyldiphenylsilyl)oxy)but-2-en-1-ol 

Downstream Products

• 905280-25-3 Benzoic acid (1S,2S)-2-(tert-butyl-diphenyl-silanyloxymethyl)-1-(R)-1,4-dioxa-spiro[4.5]dec-2-yl-4-hydroxy-butyl ester 
• 905280-26-4 Benzoic acid (1S,2S)-2-(tert-butyl-diphenyl-silanyloxymethyl)-1-(R)-1,4-dioxa-spiro[4.5]dec-2-yl-4-oxo-butyl ester 
• 905280-28-6 Acetic acid (4S,5S)-4-(tert-butyl-diphenyl-silanyloxymethyl)-5-(R)-1,4-dioxa-spiro[4.5]dec-2-yl-tetrahydro-furan-2-yl ester 
• 905280-24-2 Benzoic acid (1S,2S)-2-(tert-butyl-diphenyl-silanyloxymethyl)-1-(R)-1,4-dioxa-spiro[4.5]dec-2-yl-but-3-enyl ester 
• 905280-18-4 2-(tert-butyl-diphenyl-silanyloxymethyl)-1-(1,4-dioxa-spiro[4.5]dec-2-yl)-but-3-en-1-one 

Relevant academic research and scientific papers

A simple and stereodivergent strategy for the synthesis of 3′-C-branched 2′,3′-dideoxynucleosides exploiting (Z)-but-2-en-1,4-diol and (R)-2,3-cyclohexylideneglyceraldehyde

Barbier type additions of allylic bromide 4, derived from (Z)-but-2-en-1,4-diol 2 to (R)-2,3-cyclohexylideneglyceraldehyde 1 were performed through mediation with Zn employing Luche's procedure and also with low valent Cu, Co, and Fe which were produced v