21078-03-5Relevant articles and documents
A short, vinyl radical cyclisation approach to (±))-2-pupukeanone
Srikrishna,Vijaykumar,Sharma
, p. 2003 - 2004 (1997)
Addition of tri-n-butyltin radical to a 5-(prop-2-ynyl)bicyclo [2.2.2]oct-2-ene followed by 5-exo-trig cyclisation of the resulting vinyl radical furnishes an isotwistane, providing a short route to the sesquiterpenes, pupukeananes 4 and 2.
Method for synthesizing mexiletine chloride
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Paragraph 0031; 0032; 0033; 0034, (2019/03/15)
The invention discloses a method for synthesizing mexiletine chloride, wherein a reaction system takes 2,6-xylenol as a starting material to synthesize a corresponding target product. In the reaction,a transition metal gold complex and a ruthenium complex are used for catalysis, compared with the previous method for synthesizing mexiletine chloride, no alkali is added during a reaction process, no by-products are produced, the reaction atom economy is high, and the reaction conditions are mild. Therefore, the method has broad development prospects.
Formal total synthesis of 2-pupukeanone via radical mediated cyclisation of an enyne
Srikrishna,Vijaykumar,Sharma
, p. 766 - 770 (2007/10/03)
Diels-Alder reaction of the dienone 12, obtained by C-alkylation of sodium 2,6-dimethylphenoxide, with acrylonitrile and phenyl vinyl sulfones generate the enynes 14 and 17. Tributyltin radical addition to the terminal acetylene in 14 and 17 lead to the v