122172-38-7

Upstream product

• 2244-16-8 (S)-p-mentha-6,8-dien-2-one 
• 115540-13-1 Acetic acid (1S,2R,4S,6S)-2-ethynyl-4-[1-methoxy-1-(4-nitro-benzoylperoxy)-ethyl]-1-methyl-7-oxa-bicyclo[4.1.0]hept-2-yl ester 
• 39903-97-4 (S)-carvone oxide 
• 115540-12-0 Acetic acid (1S,2R,4S,6S)-2-ethynyl-4-(1-hydroperoxy-1-methoxy-ethyl)-1-methyl-7-oxa-bicyclo[4.1.0]hept-2-yl ester 
• 115540-14-2 (1S,2R,4S,6S)-2,4-diacetoxy-2-ethynyl-1-methyl-7-oxabicyclo<4.1.0>heptane 
• 115540-11-9 (1S,2R,4S,6S)-2-acetoxy-2-ethynyl-4-isopropenyl-1-methyl-7-oxabicyclo<4.1.0>heptane 
• 115540-15-3 (1S,5R)-5-acetoxy-1-ethynyl-3-hydroxy-2-methylcyclohex-1-ene 
• 115540-10-8 (1S,2R,4S,6S)-2-ethynyl-2-hydroxy-4-isopropenyl-1-methyl-7-oxabicyclo<4.1.0>heptane 
• 113375-51-2 (3S,5R)-1-ethynyl-3,5-dihydroxy-2-methylcyclohex-1-ene 
• 83076-51-1 de-A,B-25-cholesten-8-one 
• 116531-17-0 de-A,B-cholesta-9⁽¹¹⁾,25-dien-8-one 
• 116506-67-3 TB 

Downstream Products

• 122172-39-8 (1S,3S)-bis<(tert-butyldimethylsilyl)oxy>-9,10-secocholesta-5(10),9(11),25-trien-6-yn-8β-yl benzoate 

Relevant academic research and scientific papers

Synthesis and Biological Activity of 9,11-Dehydrovitamin D3 analogues: Stereoselctive Preparation of 6β-Vitamin D Vinylallenes and a Concise Enynol Synthesis for Preparing the A-Ring

The Δ9(11)-unsaturated vitamin D analogues 5a and 5b are of biochemical interest because they are incapable of tautomerizing via a sigmatropic hydrogen shift to a previtamin structure related to 3 and also becouse they possess a perturbed