A methodology for the synthesis of compounds containing the cis-anti-cis fused triquinane system has been developed starting from tricyclo[5.2. 1.0(2.6)]deca-4,8-dien-3-(exo)ol 6 involving Ireland ester Claisen rearrangement and intramolecular diazo ketone cyclopropanation reactions as key steps
Key Word Index-Albene; quaternary carbons; Claisen rearrangement; diazo ketone; cyclopropana-tion; r...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Oxabicyclononene I (RR1 = CH2CH:CHCH2) underwent ozonolysis to give the diacid I (R = R1 = CH2CO2H) ...
A methodology for the synthesis of compounds containing the cis-anti-cis fused triquinane system has...
The enantioselective syntheses of diquinane and cis, anti, cis-linear triquinanes, starting from the...
A novel, general, and stereoselective route for rapid creation of functionalized, linearly fused cis...
A new stereoselective synthesis of linearly fused triquinane intermediate from a simple aromatic pre...
Pentalenic acid, 5, and pentalenene, 4, and their C-9 epimers 5a and 4a, respectively, were synthesi...
Functionalized cis-syn-cis triquinane ring systems are identified as useful precursors to higher pol...
A new synthetic strategy for natural triquinanes is presented as a model study. Stereospecific rearr...
[[abstract]]Angularly and linearly fused triquinanes 10 and 15 were synthesized from catechol deriva...
A simple approach to the synthesis of a key intermediate containing the cis-anti-cis linear triquina...
Starting from 4-substituted cyclohexanones, a practical synthetic route to enantiopure 6-substituted...
Department of Organic Chemistry, Indian Institute of Science, Bangalore-560 012 Manuscript received...
Tandem radical cyclization to vinylogous carbonates and carbamates is developed for a new, highly st...
Key Word Index-Albene; quaternary carbons; Claisen rearrangement; diazo ketone; cyclopropana-tion; r...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Oxabicyclononene I (RR1 = CH2CH:CHCH2) underwent ozonolysis to give the diacid I (R = R1 = CH2CO2H) ...
A methodology for the synthesis of compounds containing the cis-anti-cis fused triquinane system has...
The enantioselective syntheses of diquinane and cis, anti, cis-linear triquinanes, starting from the...
A novel, general, and stereoselective route for rapid creation of functionalized, linearly fused cis...
A new stereoselective synthesis of linearly fused triquinane intermediate from a simple aromatic pre...
Pentalenic acid, 5, and pentalenene, 4, and their C-9 epimers 5a and 4a, respectively, were synthesi...
Functionalized cis-syn-cis triquinane ring systems are identified as useful precursors to higher pol...
A new synthetic strategy for natural triquinanes is presented as a model study. Stereospecific rearr...
[[abstract]]Angularly and linearly fused triquinanes 10 and 15 were synthesized from catechol deriva...
A simple approach to the synthesis of a key intermediate containing the cis-anti-cis linear triquina...
Starting from 4-substituted cyclohexanones, a practical synthetic route to enantiopure 6-substituted...
Department of Organic Chemistry, Indian Institute of Science, Bangalore-560 012 Manuscript received...
Tandem radical cyclization to vinylogous carbonates and carbamates is developed for a new, highly st...
Key Word Index-Albene; quaternary carbons; Claisen rearrangement; diazo ketone; cyclopropana-tion; r...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Oxabicyclononene I (RR1 = CH2CH:CHCH2) underwent ozonolysis to give the diacid I (R = R1 = CH2CO2H) ...
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