1334404-63-5

Upstream product

• 1374424-29-9 C₉H₁₆OS₂ 
• 1374424-66-4 C₉H₁₆OS₂ 
• 1334404-59-9 C₃₆H₄₉NO₅SSi 
• 1334404-57-7 C₃₂H₄₃NO₄SSi 
• 1334404-45-3 2-[2-((tert-butyl)diphenylsilanyloxy)ethyl]-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydropyridine 
• 1334404-44-2 (R)-N-(1-[2-((tert-butyl)diphenylsilanyloxy)ethyl]-4-[1,3]dioxolan-2-ylbutyl)-4-methylbenzenesulfonamide 
• 1334404-62-4 4-((2S,3R,6S)-6-(2-((tert-butyl)diphenylsilyloxy)ethyl)-3-methylpiperidin-2-yl)butan-1-ol 
• 1334404-60-2 4-((2S,3R,6S)-6-(2-((tert-butyl)diphenylsilyloxy)ethyl)-3-methyl-1-tosylpiperidin-2-yl)butan-1-ol 
• 1334404-58-8 (-)-(E)-methyl 4-((2S,3R,6S)-6-(2-((tert-butyl)diphenylsilyloxy)ethyl)-3-methyl-1-tosylpiperidin-2-yl)but-2-enoate 
• 1334404-56-6 (2S,3R,6S)-6-(2-((tert-butyl)diphenylsilyloxy)ethyl)-3-(iodomethyl)-2-methoxy-1-tosylpiperidine 
• 1334404-53-3 (-)-(1R,3S,6S)-3-(2-((tert-butyl)diphenylsilyloxy)ethyl)-2-tosyl-2-azabicyclo[4.1.0]heptane 

Relevant academic research and scientific papers

A Stereoselective Formal Synthesis of Quinolizidine (–)-217A

The stereoselective formal synthesis of quinolizidine alkaloid (–)-217A was achieved by utilizing a combination of the dithiane coupling reaction and the organocatalytic aza-conjugate addition reaction promoted by the gem-disubstituent effect to provide t

Stereoselective approaches to 2,3,6-trisubstituted piperidines. An enantiospecific synthesis of quinolizidine (-)-217A

The enantiospecific and diastereocontrolled total synthesis of alkaloid (-)-217A is described that employs a stepwise [3+3] annelation strategy and a piperidine 2,3-cyclopropanation-ring opening reaction as the key steps.