203307-23-7

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 

Downstream Products

• 203307-24-8 (S)-1-(tert-Butyl-dimethyl-silanyloxy)-7-(4-methoxy-benzyloxy)-6-(tetrahydro-pyran-2-yloxy)-hept-4-yn-2-ol 
• 203307-26-0 tert-Butyl-[(S)-6-(4-methoxy-benzyloxy)-5-(tetrahydro-pyran-2-yloxy)-hex-3-ynyloxy]-diphenyl-silane 
• 203307-28-2 (Z)-(S)-6-(tert-Butyl-diphenyl-silanyloxy)-4-chloro-1-(4-methoxy-benzyloxy)-hex-3-en-2-ol 
• 203307-27-1 (S)-6-(tert-Butyl-diphenyl-silanyloxy)-1-(4-methoxy-benzyloxy)-hex-3-yn-2-ol 
• 203307-31-7 (S)-7-(4-Methoxy-benzyloxy)-6-(tetrahydro-pyran-2-yloxy)-hept-4-yne-1,2-diol 
• 203307-25-9 (S)-6-(4-Methoxy-benzyloxy)-5-(tetrahydro-pyran-2-yloxy)-hex-3-yn-1-ol 

Relevant academic research and scientific papers

Absolute stereocmemistry of halichlorine; a potent inhibitor of VCAM-1 induction

The absolute stereochemistry of a marine alkaloid halichlorine, which significantly inhibits VCAM-1 induction in HUVE cells, was established by synthesis of a degradation product of natural product.