We report a highly diastereoselective approach for the synthesis of the pentacyclic indole core of the manadomanzamine alkaloid skeleton, with complete control over the relative and absolute stereochemistries at the three contiguous stereocentres at ring positions 1, 10, and 24, from a readily available chiral template. Crown Copyright (c) 2007 Published by Elsevier Ltd. All rights reserved
This thesis describes our efforts towards the total synthesis of natural products and the developmen...
The asperparalines belong to a large family of prenylated indole alkaloids possessing a characterist...
We have developed a new and highly stereoselective approach to indolizino[8,7-b]indole derivatives s...
We report a highly diastereoselective approach for the synthesis of the pentacyclic indole core of t...
We report a highly diastereoselective approach for the synthesis of a functionalized dodecahydrobenz...
Towards a total synthesis of the manadomanzamine alkaloids: the first asymmetric construction of the...
Total asymmetric syntheses of the target alkaloids are reported. The syntheses involve the preparati...
The total synthesis of a variety of indole and dihydroindole alkaloids, is described. Mere specifica...
An enantioselective total synthesis of (-)-terengganensine A, a heptacyclic monoterpene indole alkal...
A full account of our studies toward reverse-prenylated indole alkaloids that contain a bicyclo[2.2....
Indolin-3-ones with a chiral center at the 2-position are encountered in a large variety of natural ...
The first regio- and stereocontrolled total synthesis of the bisphenolic, bisquaternary alkaloid (+)...
Schiff bases derived from tryptophan methyl ester react with differently substituted electron-rich s...
An efficient enantioselective 12-step synthesis of the ABCDE pentacyclic core of the Strychnos alkal...
We report herein the enantioselective total synthesis of three monoterpene indole alkaloids, namely,...
This thesis describes our efforts towards the total synthesis of natural products and the developmen...
The asperparalines belong to a large family of prenylated indole alkaloids possessing a characterist...
We have developed a new and highly stereoselective approach to indolizino[8,7-b]indole derivatives s...
We report a highly diastereoselective approach for the synthesis of the pentacyclic indole core of t...
We report a highly diastereoselective approach for the synthesis of a functionalized dodecahydrobenz...
Towards a total synthesis of the manadomanzamine alkaloids: the first asymmetric construction of the...
Total asymmetric syntheses of the target alkaloids are reported. The syntheses involve the preparati...
The total synthesis of a variety of indole and dihydroindole alkaloids, is described. Mere specifica...
An enantioselective total synthesis of (-)-terengganensine A, a heptacyclic monoterpene indole alkal...
A full account of our studies toward reverse-prenylated indole alkaloids that contain a bicyclo[2.2....
Indolin-3-ones with a chiral center at the 2-position are encountered in a large variety of natural ...
The first regio- and stereocontrolled total synthesis of the bisphenolic, bisquaternary alkaloid (+)...
Schiff bases derived from tryptophan methyl ester react with differently substituted electron-rich s...
An efficient enantioselective 12-step synthesis of the ABCDE pentacyclic core of the Strychnos alkal...
We report herein the enantioselective total synthesis of three monoterpene indole alkaloids, namely,...
This thesis describes our efforts towards the total synthesis of natural products and the developmen...
The asperparalines belong to a large family of prenylated indole alkaloids possessing a characterist...
We have developed a new and highly stereoselective approach to indolizino[8,7-b]indole derivatives s...