790662-54-3

Upstream product

• 505-23-7 1,3 dithiane 
• 183894-33-9 (R)-(+)-1-[(3'-iodo-2'-methylpropoxy)methyl]-4-methoxybenzene 

Downstream Products

• 790662-57-6 (2S,3R,5R,2'S,1''R)-1''-(3-(hydroxydimethylsilanyl)-5-{2-[3'-(4-methoxybenzyloxy)-2'-methylpropyl][1,3]dithian-2-ylmethyl}tetrahydrofuran-2-yl)prop-2''-yn-1''-ol 
• 790662-56-5 (2S,3R,5R,2'S,1''R)-1''-{(3-(dimethylphenylsilanyl)-5-{2-[3'-(4-methoxybenzyloxy)-2'-methylpropyl][1,3]dithian-2-ylmethyl}tetrahydrofuran-2-yl)}prop-2''-yn-1''-ol 
• 790662-67-8 (2S,3R,5R,1'R,2''S)-2-[1'-(tert-butyldimethylsilanyloxy)-3'-(triethylsilanyl)prop-2'-ynyl]-3-(dimethylphenylsilanyl)-5-{2-[3''-(4-methoxybenzyloxy)-2''-methylpropyl][1,3]dithian-2-ylmethyl}tetrahydrofuran 

Relevant academic research and scientific papers

Synthesis of the C11-C29 fragment of amphidinolide F

(Chemical Equation Presented) An efficient synthesis of the C(11)-C(29) fragment 31 of amphidinolide F has been accomplished via a diastereoselective [3 + 2]-annulation reaction of allylsilane 5 and ethyl glyoxylate to prepare the key tetrahydrofuran 15 a