Both liquid and solid hexahydrocostunolides obtained by the pressure hydrogenation of costunolide (V) and solid dihydrocostunolide (VI) respectively, give the same optically active hexahydrogermacol (IIIa), when subjected to controlled reduction with LiAlH4, followed by Huang-Minlon reduction. The alcohol (IIIa) on oxidation with chromic oxide gives optically active hexahydrogermacrone (IIa). Dehydration of IIIa with KHSO4 followed by catalytic hydrogenation gives the optically inactive saturated hydrocarbon, germacrane (IV). Since the total synthesis of solid dihydrocostunolide (VI) has already been achieved the preparation of IIIa, IIa and IV from VI constitutes a total synthesis of the above three compounds
Department of Chemistry, Panjab University, Chandigarh-160014 Manuscript received 28 February 1975 ...
In this thesis, the synthesis of a number of germacrane sesquiterpenes is described. Functionalized ...
A sequence leading to the total synthesis of certain derivatives in the 11, 12-seco (see XXIV) and 5...
A review is presented of the various methods for the preparation of germacrane sesquiterpenes and re...
Tetrahydroelemol and dihydroeudesmol undergo dehydration on treatment with traces of perchloric acid...
The terpenes constitute an important group amongst the naturally occurring organic compounds. They v...
Dihydroselinene (VII), obtained by the pyrolysis of dihydroeudesmol benzoate (VI) on hydroboration-o...
Solid dihydrocostunolide (VI), on metal-amine reduction furnishes an acid, C15H24O2 (VII; R = H), th...
Department of Chemistry, Panjab University, Chandigarh-160014. Manuscript received 26 August 1974 ;...
In this thesis, the synthesis of a number of germacrane sesquiterpenes is described. Functionalized ...
Department of Chemistry, Panjab University, Chandigarh-14 Manuscript received 16 August 1972; accep...
2-Methyl-6, 6-ethylenedioxy-2-2 heptanol, obtained through hydration of 2-methyl-6, 6-ethylenedioxy-...
An efficient method has been developed for the synthesis of (E,E)-germacrane sesquiterpene alcohols....
α-cyclocostunolide (IV), a product of transannular crystaliaton of costunolide, gives, on treatment ...
Starting from trans-geranylacetone, obtained through the Claisen rearrangement of properly substitut...
Department of Chemistry, Panjab University, Chandigarh-160014 Manuscript received 28 February 1975 ...
In this thesis, the synthesis of a number of germacrane sesquiterpenes is described. Functionalized ...
A sequence leading to the total synthesis of certain derivatives in the 11, 12-seco (see XXIV) and 5...
A review is presented of the various methods for the preparation of germacrane sesquiterpenes and re...
Tetrahydroelemol and dihydroeudesmol undergo dehydration on treatment with traces of perchloric acid...
The terpenes constitute an important group amongst the naturally occurring organic compounds. They v...
Dihydroselinene (VII), obtained by the pyrolysis of dihydroeudesmol benzoate (VI) on hydroboration-o...
Solid dihydrocostunolide (VI), on metal-amine reduction furnishes an acid, C15H24O2 (VII; R = H), th...
Department of Chemistry, Panjab University, Chandigarh-160014. Manuscript received 26 August 1974 ;...
In this thesis, the synthesis of a number of germacrane sesquiterpenes is described. Functionalized ...
Department of Chemistry, Panjab University, Chandigarh-14 Manuscript received 16 August 1972; accep...
2-Methyl-6, 6-ethylenedioxy-2-2 heptanol, obtained through hydration of 2-methyl-6, 6-ethylenedioxy-...
An efficient method has been developed for the synthesis of (E,E)-germacrane sesquiterpene alcohols....
α-cyclocostunolide (IV), a product of transannular crystaliaton of costunolide, gives, on treatment ...
Starting from trans-geranylacetone, obtained through the Claisen rearrangement of properly substitut...
Department of Chemistry, Panjab University, Chandigarh-160014 Manuscript received 28 February 1975 ...
In this thesis, the synthesis of a number of germacrane sesquiterpenes is described. Functionalized ...
A sequence leading to the total synthesis of certain derivatives in the 11, 12-seco (see XXIV) and 5...