105676-53-7

Upstream product

• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 

Downstream Products

• 115479-71-5 (4R,5R,7S)-9-(tert-Butyl-diphenyl-silanyloxy)-4-hydroxy-5,7-dimethyl-2-phenylselanyl-nonanoic acid 
• 115479-72-6 (R)-5-[(1R,3S)-5-(tert-Butyl-diphenyl-silanyloxy)-1,3-dimethyl-pentyl]-3-phenylselanyl-dihydro-furan-2-one 
• 105676-22-0 Methanesulfonic acid (Z)-(1S,2R,3R,4R,8R,10R)-3,11-bis-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-2,4,8,10-tetramethyl-undec-5-enyl ester 
• 105676-21-9 (Z)-(2S,3S,4R,5R,9R,11R)-4,12-Bis-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-3,5,9,11-tetramethyl-dodec-6-en-2-ol 
• 105676-19-5 (S)-4-((Z)-(1R,2R,3R,7R,9R)-2,10-Bis-benzyloxy-1,3,7,9-tetramethyl-dec-4-enyl)-2,2-dimethyl-[1,3]dioxolane 
• 105676-20-8 (Z)-(2S,3S,4R,5R,9R,11R)-4,12-Bis-benzyloxy-3,5,9,11-tetramethyl-dodec-6-ene-1,2-diol 
• 105676-23-1 (R)-2-((Z)-(1R,2R,3R,7R,9R)-2,10-Bis-benzyloxy-1,3,7,9-tetramethyl-dec-4-enyl)-oxirane 
• 105676-24-2 ((3S,5R)-6-Benzyloxy-3,5-dimethyl-hexyloxy)-tert-butyl-diphenyl-silane 
• 105676-57-1 (2R,4S)-6-(tert-butyldiphenylsilanyloxy)-2,4-dimethylhexanal 
• 105676-28-6 C₂₁H₂₈O₃S 
• 105676-58-2 (2R,4S)-6-(tert-butyldiphenylsilanyloxy)-2,4-dimethylhexan-1-ol 
• 105676-27-5 C₂₁H₂₈OS 
• 105676-26-4 Methanesulfonic acid (3S,5R)-6-benzyloxy-3,5-dimethyl-hexyl ester 
• 105676-25-3 (3S,5R)-6-Benzyloxy-3,5-dimethyl-hexan-1-ol 

Relevant academic research and scientific papers

STEREOCHEMICAL CONTROL OF NATURE'S BIOSYNTHETIC PATHWAYS: A GENERAL STRATEGY FOR THE SYNTHESIS OF POLYPROPIONATE-DERIVED STRUCTURAL UNITS FROM A SINGLE CHIRAL PROGENITOR

A general strategy that permits the stereocontrolled construction of acyclic chains containing vicinal and/or alternating alkyl and hydroxy substituents is presented.Structural subunits of ionomycin were synthesized from a common chiral intermediate.