1196718-45-2

Upstream product

• 1066-54-2 trimethylsilylacetylene 
• 128461-65-4 3-(p-methoxybenzyloxy)propanal 
• 1195470-99-5 5-(4-methoxybenzyloxy)-1-trimethylsilylpent-1-yne-3-ol 
• 1195470-78-0 1-trimethylsilyl-5-(4-methoxybenzyloxy)-1-pentyn-3-one 

Downstream Products

• 1300117-39-8 N-benzyl-N-{(E)-(3S)-[2-((3aR,8aS)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-oxoethoxy]-5-(4-methoxybenzyloxy)pent-1-enyl}-4-methylbenzenesulfonamide 
• 1300117-42-3 N-benzyl-N-{(1R)-1-[(1S)-1-hydroxy-2-oxo-2-((3aR,8aS)-2,2-dimethyl-8,8adihydro-3aH-indeno[1,2-d]oxazol-3-yl)ethyl]-5-(4-methoxybenzyloxy)pent-2-enyl}-4-methylbenzenesulfonamide 
• 1300117-44-5 methyl (2S,3R)-3-[benzyl(4-methylbenzenesulfonyl)amino]-2,7-dihydroxy-hept-4-enoate 
• 1300117-45-6 methyl (2S,3R)-3-[benzyl(4-methylbenzenesulfonyl)amino]-2,7-di(tert-butyldimethylsilyloxy)hept-4-enoate 
• 1300117-47-8 (3S,4R)-1-benzyl-3-(tert-butyldimethylsilyl)oxy-4-{(E)-4-[(tert-butyldimethylsilyl)oxy]-but-1-enyl}azetidin-2-one 
• 1300117-46-7 methyl (2S,3R)-3-benzylamino-(2,7)-[di(tert-butyldimethylsilyl)oxy]hept-4-enoate 
• 1300116-95-3 N-benzyl-N-[(3S)-3-hydroxy-5-(4-methoxybenzyloxy)pent-1-ynyl]-4-methylbenzenesulfonamide 
• 1300116-96-4 N-[(3S)-3-hydroxy-4-(4-methoxybenzyloxy)pent-1-ynyl]-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide 
• 1300116-88-4 (3S)-1-bromo-3-(tert-butyldiphenylsilyloxy)-5-(4-methoxybenzyloxy)pent-1-yne 
• 1300116-91-9 N-benzyl-N-{(3S)-3-[(tert-butyldiphenylsilyl)oxy]-5-(4-methoxybenzyloxy)pent-1-ynyl}-4-methylbenzenesulfonamide 
• 1300116-92-0 (S)-N-{(3S)-3-[(tert-butyldiphenylsilyl)oxy]-4-(4-methoxybenzyloxy)pent-1-ynyl}-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide 
• 1300116-98-6 N-benzyl-N-[(E)-(3S)-3-hydroxy-5-(4-methoxybenzyloxy)pent-1-enyl]-4-methylbenzenesulfonamide 
• 1300116-99-7 N-[(E)-(3S)-3-hydroxy-4-(4-methoxybenzyloxy)pent-1-enyl]-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide 
• 1300116-87-3 (3S)-3-(tert-butyldiphenylsilyloxy)-5-(4-methoxybenzyloxy)-1-trimethylsilylpent-1-yne 

Relevant academic research and scientific papers

Synthesis of 1,2-amino alcohols by sigmatropic rearrangements of 3-(N-Tosylamino)allylic alcohol derivatives

Sigmatropic rearrangements of 3-(N-tosylamino)allylic alcohol derivatives, a particular subclass of functionalized enamides, have been investigated. Whereas the presence of the nitrogen atom alters the stereochemical outcome of Ireland-Claisen rearrangeme