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Breakthrough in the synthesis of fungal bioactive compounds for therapeutic applications - MSNTo make the aldehyde (5), dinitrile (6) was first converted into diester. Then, the hydroxy groups in diester were protected with a tert-butyldiphenylsilyl (TBDPS) group to form protected ether.
Initial attempts on intramolecular α-cyclopropanation. Enantioselective α-halogenation of aldehydes have been reported by several research groups 47,48,49,50,51,52,53,54,55,56.Among those ...
This video shows a fleeting hemiacetal alkoxide intermediate, which the researchers, unprecedentedly, captured. The team also observed its reverse aldehyde elimination, generating an aldehyde ...
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