756524-19-3

Upstream product

• 142860-84-2 4-(p-methoxybenzyloxy)-1,2-epoxybutane 
• 756523-94-1 7-(tert-butyl-dimethyl-silanyloxy)-1-(4-methoxy-benzyloxy)-hept-5-yn-3-ol 
• 756523-97-4 Acetic acid (S)-1-((2S,3R)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester 
• 756523-95-2 Acetic acid (Z)-(R)-5-hydroxy-1-[2-(4-methoxy-benzyloxy)-ethyl]-pent-3-enyl ester 

Downstream Products

• 756523-92-9 (9Z,11E)-(4S,6S,8R)-17-(tert-Butyl-dimethyl-silanyloxy)-4-[2-(4-methoxy-benzyloxy)-ethyl]-3,7-dioxa-tricyclo[11.4.0.0^6,8]heptadeca-1⁽¹⁷⁾,9,11,13,15-pentaen-2-one 
• 756523-88-3 2-(tert-Butyl-dimethyl-silanyloxy)-6-((1E,3Z)-penta-1,3-dienyl)-benzoic acid (S)-1-[(2S,3R)-((Z)-3-hepta-1,6-dienyl)-oxiranylmethyl]-3-(4-methoxy-benzyloxy)-propyl ester 
• 756524-26-2 2-(tert-Butyl-dimethyl-silanyloxy)-6-((1E,3Z)-5-methyl-hexa-1,3-dienyl)-benzoic acid (S)-1-[(2S,3R)-((Z)-3-hepta-1,6-dienyl)-oxiranylmethyl]-3-(4-methoxy-benzyloxy)-propyl ester 

Relevant academic research and scientific papers

Total synthesis of the salicylate enamide macrolide oximidine III: Application of relay ring-closing metathesis

The vacuolar-type (H+)-adenosine triphosphatase inhibitor oximidine III and its enamide and epoxide stereoisomers have been synthesized enantioselectively. A relay ring-closing metathesis (RCM) strategy was employed to facilitate the macrocycli