Paper Title :Synthesis of Hydrogenated Isozonarol via Diels Alder Reaction: A Convergent Approach to ABC Tricyclic Core of Marine Sesquiterpenoids
Author :Preeti Zade , S N Zade, M M V Ramana
Article Citation :Preeti Zade ,S N Zade ,M M V Ramana ,
(2019 ) " Synthesis of Hydrogenated Isozonarol via Diels Alder Reaction: A Convergent Approach to ABC Tricyclic Core of Marine Sesquiterpenoids " ,
International Journal of Advances in Science, Engineering and Technology(IJASEAT) ,
pp. 35-39,
Volume-7,Issue-3
Abstract : The synthesis of natural products plays an important role in organic and biological chemistry. These compounds show a great variety of chemical structures and a wide range of biological activities1. The synthetic utility and potential power of the Diels–Alder reaction2 in organic chemistry is evident. The present paper relates to the synthesis of dihydroisozonarol by [4+2] cycloaddition reaction between 1,3,3-trimethyl-2-vinyl-1-cyclohexene and (E)-1-(2,5-dimethoxyphenyl) but-2-en-1-one followed by hydrogenation and demethylation. Keywords - Sesquiterpenoids, Cylcoaddition, Diels Alder reaction
Type : Research paper
Published : Volume-7,Issue-3
DOIONLINE NO - IJASEAT-IRAJ-DOIONLINE-16118
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Published on 2019-11-18 |
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