130497-99-3

Upstream product

• 80684-00-0 tert-butyl dimethyl(pent-3-en-1-yloxy)silane 
• 39161-19-8 pent-3-en-1-ol 
• 191410-11-4 (S)-3-(4-Methoxy-benzyloxy)-4-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-butan-1-ol 
• 191410-04-5 Acetic acid (4R,6R,7R)-6-(tert-butyl-dimethyl-silanyloxy)-7-methyl-2-oxo-oxepan-4-yl ester 
• 191410-09-0 (S)-4-((4R,5R)-2,2,5-Trimethyl-[1,3]dioxolan-4-yl)-butane-1,3-diol 
• 191410-08-9 (3S,5R,6R)-Heptane-1,3,5,6-tetraol 
• 106987-88-6 2-[(4R,5R)-2,2,5-trimethyl-1,3-dioxolan-4-yl]-1-ethanol 
• 818-58-6 methyl (E)-pent-3-enoate 
• 764-37-4 (E)-3-penten-1-ol 
• 824-94-2 p-methoxybenzyl chloride 
• 111043-64-2 (4S,6R,7R)-6,7-di-O-isopropylideneoct-1-yn-4-ol 
• 325706-85-2 (3R,4R)-3,4-di-O-isopropylidene-1-tert-butyldimethylsilyloxypentane 
• 325706-77-2 (2R,3R)-5-tert-butyldimethylsilyloxypentane-2,3-diol 
• 325706-76-1 (E)-pent-3-en-1-ol tert-butyldimethylsilyl ether 

Downstream Products

• 325706-83-0 (S)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-eth-(Z)-ylidene]-7-(4-methoxy-benzyloxy)-2,2-dimethyl-1-phenylsulfanyl-8-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-octan-3-ol 
• 325706-75-0 (7S,9R,10R)-5-[(E)-2-tert-butyldiphenylsilyloxyethylidene]-7-(4-methoxybenzyloxy)-2,2-dimethyl-1-phenylsulfanyl-9,10-di-O-isopropylideneundecan-3-one 
• 325706-80-7 (2E,5R,7R,8R)-3-bromo-1-tert-butyldiphenylsilyloxy-7,8-di-O-isopropylidene-5-(4-methoxybenzyloxy)non-2-ene 
• 130498-00-9 methyl (5S,7R,8R)-7,8-di-O-isopropylidene-5-(4-methoxybenzyloxy)non-2-ynoate 

Relevant academic research and scientific papers

Syntheses of C17-C27 fragments of 20-deoxybryostatins for assembly using Julia and metathesis reactions

Two approaches to the synthesis of compounds corresponding to the C17-C27 fragment of the 20-deoxybryostatins are described. The first approach is based on the palladium(0) catalysed coupling of tin enolates, generated in situ from enol acetates using tri

Synthesis of the C(17)-C(27) fragment of the 20-deoxybryostatins

A synthesis of the C(17)-C(27) fragment of the 20-deoxybryostatins is described in which the key step is a palladium(0) catalysed coupling of a tributyltin enolate with a vinylic bromide. (C) 2000 Elsevier Science Ltd.

(R)-Carvone as chiral template for the synthesis of some polyols

Some (4S,6R,7R) 4,6,7-trihydroxyheptyl derived building blocks have been obtained from (R)-carvone as the chiral template.A key-step is the Baeyer-Villiger oxidation of a suitable intermediate.