(1S,2S,3R,5S)-(+)-Pinanediol

(1S,2S,3R,5S)-(+)-2,3-Pinanediol finds applications across multiple fields:

• Chiral Reagent: It serves as a chiral reagent in the synthesis of homochiral α-hydroxyketones and the resolution of prolineboronate esters.
• Pharmaceuticals: Its biological properties make it a candidate for drug development aimed at cancer therapies and neuroprotective agents.
• Cosmetics: The compound is utilized in formulations for sunless tanning products due to its effect on melanin production.

Research indicates that (1S,2S,3R,5S)-(+)-2,3-Pinanediol exhibits significant biological activity. It has been shown to induce differentiation in S91 melanoma and PC12 pheochromocytoma cells, suggesting potential therapeutic applications in cancer treatment and neuroprotection. Additionally, its structure allows it to interact with biological systems in ways that could lead to the development of sunless tanning products due to its ability to influence melanin production.

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