99017-80-8

Upstream product

• 17690-16-3 benzyl bromomethyl ether 
• 105-45-3 acetoacetic acid methyl ester 

Downstream Products

• 104713-29-3 (3R)-hydroxy-5-benzyloxy-pentanoic acid methyl ester 
• 99606-36-7 2-[2-(2-Benzyloxy-ethyl)-4-oxo-azetidin-1-yl]-2-hydroxy-malonic acid diethyl ester 
• 99606-31-2 O-benzyl 3-hydroxy-5-(benzyloxy)pentahydroxamate 
• 99606-32-3 4-<2-(benzyloxy)ethyl>-N-(benzyloxy)-2-azetidinone 
• 99617-58-0 3-hydroxy-5-(benzyloxy)pentanoic cid 
• 99606-33-4 4-<2-(benzyloxy)ethyl>-N-hydroxy-2-azetidinone 
• 99606-35-6 4-<2-(benzyloxy)ethyl>-2-azetidinone 
• 162600-54-6 cryptophycin-24 
• 219606-86-7 tert-butyl (5S,6R)-5-[(2S)-2-[3-[(2R)-2-tert-butoxycarbonylamino-3-(4-methoxyphenyl)-propionylamino]propionyloxy]-4-methylpentanoyloxy]-6-methyl-8-phenylocta-2(E),7(E)-dienoate 
• 219606-79-8 tert-butyl (2E,5S,6R,7E)-5-{[tert-butyl(dimethyl)silyl]oxy}-6-methyl-8-phenylocta-2,7-dienoate 
• 188926-26-3 {(1E,3R,4S)-4,6-bis{[(tert-butyl)dimethylsilyl]oxy}-3-methylhex-1-enyl}benzene 
• 188926-22-9 methyl (2S,3S)-5-benzyloxy-3-hydroxy-2-methylpentanoate 
• 208581-50-4 (3S,4R,5E)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-methyl-6-phenylhex-5-en-1-ol 
• 178977-57-6 tert-butyl (5S,6R,2E,7E)-5-hydroxy-6-methyl-8-phenyl-2,7-octadienoate 

Relevant academic research and scientific papers

[1,2]- or [2,3]-rearrangement of onium ylides of allyl and benzyl ethers and sulfides via in situ-generated iodonium ylides

(Chemical Equation Presented) Iodonium ylides, generated in situ with bisacetoxyiodobenzene, are converted to allyl- or benzyl-substituted oxonium or sulfonium ylides via rhodium- or copper-catalyzed carbene transfer. Except for the S-benzyl example, the