The gross mechanism of rearrangement of longifolene to isolongifolene has been elucidated by using site-specifically labelled longifolene-4, 4, 5, 5-d4 and shown to follow the pathway proposed by Berson et al., which involves an exo, exo Me shift, in preference to the endo, endo Me migration route proposed earlier. An efficient synthesis of longifolene-4, 4, 5, 5-d4, the key compound in the present investigation, is described
Dehydrogenation of isolongifolene over 10% Pd-C, in the vapour phase, at 450-±5° gave in 23% yield a...
Isolongifolene has been systematically degraded to a bisnor-keto acid, the spectral characteristics ...
Terpenes constitute the largest class of natural products and serve as an important source for medic...
The gross mechanism of rearrangement of longifolene to isolongifolene has been elucidated by using s...
The question of possible neutral intermediates which may lie on the reaction pathway in going from l...
Isolongifolene, C15H24 an artefact from an acid-catalysed rearrangement of longifolene, is shown to ...
Isolongifolene, C15H24 an artefact from an acid-catalysed rearrangement of longifolene, is shown to ...
Isolongifolene epoxide undergoes novel rearrangements on treatment with 1% HCl in CHCl<SUB>3</SUB> o...
Acetolysis of 8-bromoneoisolongifolene generates, besides two normal products (of elimination and SN...
Acetolysis of 8-bromoneoisolongifolene generates, besides two normal products (of elimination and SN...
Starting with camphene-1-carboxylic acid (III), both C13-keto acid (II), the key degradation product...
Longipinene on exposure to acids rapidly rearranges to furnish α- and β-himachalenes, longifolene an...
National Chemical Laboratory, Poona, India Malti-Chem Research Centre, Nandesari, Vadodara, India ...
Longifolene in Prins reaction with formaldehyde yielded the expected ω-acetoxymethyl longifolene, wh...
The isolation and stereochemistry of 3-hydroxylongifolaldehyde (4), the missing key-compound in the ...
Dehydrogenation of isolongifolene over 10% Pd-C, in the vapour phase, at 450-±5° gave in 23% yield a...
Isolongifolene has been systematically degraded to a bisnor-keto acid, the spectral characteristics ...
Terpenes constitute the largest class of natural products and serve as an important source for medic...
The gross mechanism of rearrangement of longifolene to isolongifolene has been elucidated by using s...
The question of possible neutral intermediates which may lie on the reaction pathway in going from l...
Isolongifolene, C15H24 an artefact from an acid-catalysed rearrangement of longifolene, is shown to ...
Isolongifolene, C15H24 an artefact from an acid-catalysed rearrangement of longifolene, is shown to ...
Isolongifolene epoxide undergoes novel rearrangements on treatment with 1% HCl in CHCl<SUB>3</SUB> o...
Acetolysis of 8-bromoneoisolongifolene generates, besides two normal products (of elimination and SN...
Acetolysis of 8-bromoneoisolongifolene generates, besides two normal products (of elimination and SN...
Starting with camphene-1-carboxylic acid (III), both C13-keto acid (II), the key degradation product...
Longipinene on exposure to acids rapidly rearranges to furnish α- and β-himachalenes, longifolene an...
National Chemical Laboratory, Poona, India Malti-Chem Research Centre, Nandesari, Vadodara, India ...
Longifolene in Prins reaction with formaldehyde yielded the expected ω-acetoxymethyl longifolene, wh...
The isolation and stereochemistry of 3-hydroxylongifolaldehyde (4), the missing key-compound in the ...
Dehydrogenation of isolongifolene over 10% Pd-C, in the vapour phase, at 450-±5° gave in 23% yield a...
Isolongifolene has been systematically degraded to a bisnor-keto acid, the spectral characteristics ...
Terpenes constitute the largest class of natural products and serve as an important source for medic...