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    Home > Active Ingredient News > Drugs Articles > The Synthetic Routes of Methyl 2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)octahydropyrano[3,2-b]pyran-2-yl)acetate

    The Synthetic Routes of Methyl 2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)octahydropyrano[3,2-b]pyran-2-yl)acetate

    • Last Update: 2023-05-10
    • Source: Internet
    • Author: User
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    Methyl 2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)octahydropyrano[3,2-b]pyran-2-yl)acetate is a synthetic compound that belongs to a class of organic molecules known as pyrano[3,2-b]pyrans.
    These molecules are of interest to chemical researchers due to their unique optical and electronic properties, which make them potentially useful in a variety of applications in the chemical industry.


    One of the key features of pyrano[3,2-b]pyrans is their ability to undergo a process known as intramolecular charge transfer (ICT), which involves the transfer of electrons within the molecule.
    This property makes these compounds useful in applications such as organic light-emitting diodes (OLEDs) and solar cells, where the ability to efficiently transfer electrons is crucial.


    The synthetic route to methyl 2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)octahydropyrano[3,2-b]pyran-2-yl)acetate involves a multi-step synthesis that requires a variety of chemical reagents and equipment.


    The synthesis begins with the synthesis of a precursor compound known as tert-butyl ((2S)-2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)oxy)acetate, which is then treated with a strong acid to generate the desired alcohol group.
    This intermediate is then functionalized with a second tert-butyl group, followed by treatment with a Grignard reagent to introduce the methyl group.
    The final step involves the introduction of the carbonyl group using a reagent such as oxalyl chloride.


    The synthesis of methyl 2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)octahydropyrano[3,2-b]pyran-2-yl)acetate is a challenging synthesis due to the presence of multiple functional groups and the need for careful handling of the reagents.
    However, with proper equipment and techniques, this synthesis can be successfully accomplished in a laboratory setting.


    In conclusion, methyl 2-((2R,4aS,6S,7R,8S,8aS)-7,8-bis((tert-butyldimethylsilyl)oxy)-6-((S,E)-1-((tert-butyldimethylsilyl)oxy)-3-(trimethylsilyl)allyl)octahydropyrano[3,2-b]pyran-2-yl)acetate is a synthetic compound with interesting optical and electronic properties, making it a useful building block in the chemical industry.
    Its synthesis involves a multi-step process that requires specialized equipment and expertise, but with proper execution, this synthesis can be successfully accomplished in a laboratory setting.


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