460745-02-2

Upstream product

• 153062-86-3 (R)-tetradecane-1,2-diol 
• 460744-99-4 (R)-2-(tert-butyldimethylsilyloxy)tetradecanyl pivalate 
• 636596-48-0 (R)-2-(tert-butyldimethylsilyloxy)tetradecanol 
• 636596-47-9 (R)-2-hydroxytetradecanyl pivalate 
• 114379-26-9 (R)-2-hydroxytetradecanal tert-butyldimethylsilyl ether 
• 929915-17-3 (4S)-4-[(3'R,4'R)-4'-(tert-butyldimethylsilyloxy)-3'-hydroxy-1'-hexadecynyl]-2-phenyl-1,3-dioxolane 
• 6553-96-4 2,4,6-triisopropylphenylsulfonyl chloride 
• 460745-08-8 (2S,5R,6R)-6-(tert-butyldimethylsilyloxy)octadecane-1,2,5-triol 

Relevant academic research and scientific papers

Systematic Construction of a Monotetrahydrofuran-Ring Library in Annonaceous Acetogenins by Asymmetric Alkynylation and Stereodivergent Tetrahydrofuran-Ring Formation

All eight diastereoisomers of the monotetrahydrofuran-ring cores of annonaceous acetogenins have been synthesized through utilization of asymmetric alkynylation and stereodivergent one-pot tetrahydrofuran-ring formation. In all cases, the asymmetric alkyn

Highly stereoselective and stereodivergent synthesis of four types of THF cores in acetogenins using a C4-chiral building block

(Formula Presented) Four stereoisomers of the THF cores, synthetic intermediates of acetogenins, have been synthesized with high diastereoselectivity by asymmetric alkynylation and subsequent stereodivergent THF ring formation. The asymmetric alkynylation