Stemofoline alkaloids are promising lead structures for further development in the fields of agriculture and medicine. Here, the authors report the enantioselective total syntheses of four stemofoline alkaloids in 19 steps based on a biogenetic hypothesis
This dissertation features two projects concerning natural product synthesis and reaction developmen...
The planning and implementation of an enantioselective total synthesis of (+)-scholarisine A is pres...
Throughout history, organisms have ensured their survival by producing a wide variety of small molec...
The synthesis of the Securinega alkaloid secu’amamine E (ent–virosine A) has been accomplished for t...
The synthesis of the <i>Securinega</i> alkaloid secu’amamine E (<i>ent</i>-virosine A) has been acco...
The chirality of a starting material having a chiral sp3-carbon can be preserved under some circumst...
We report herein the enantioselective total synthesis of three monoterpene indole alkaloids, namely,...
International audienceWe report the enantioselective total syntheses of mavacurans alkaloids, (+)-ta...
Stemona alkaloids, are structurally complex and polycyclic alkaloids, obtained from a novel class of...
Part one of this dissertation describes the synthesis of novel polycyclic natural product-like compo...
Strictosidine synthase triggers the formation of strictosidine from tryptamine and secologanin, ther...
A formal enantioselective total synthesis of bisdehydroneostemoninine employing L-glutamic acid as t...
The first chapter introduces the reader to the concept of natural product total synthesis and its ...
Total synthesis of natural products with diverse architecture and varying degree of complexity is an...
The isoquinoline alkaloids form a unique class of compounds, exhibiting biological properties almost...
This dissertation features two projects concerning natural product synthesis and reaction developmen...
The planning and implementation of an enantioselective total synthesis of (+)-scholarisine A is pres...
Throughout history, organisms have ensured their survival by producing a wide variety of small molec...
The synthesis of the Securinega alkaloid secu’amamine E (ent–virosine A) has been accomplished for t...
The synthesis of the <i>Securinega</i> alkaloid secu’amamine E (<i>ent</i>-virosine A) has been acco...
The chirality of a starting material having a chiral sp3-carbon can be preserved under some circumst...
We report herein the enantioselective total synthesis of three monoterpene indole alkaloids, namely,...
International audienceWe report the enantioselective total syntheses of mavacurans alkaloids, (+)-ta...
Stemona alkaloids, are structurally complex and polycyclic alkaloids, obtained from a novel class of...
Part one of this dissertation describes the synthesis of novel polycyclic natural product-like compo...
Strictosidine synthase triggers the formation of strictosidine from tryptamine and secologanin, ther...
A formal enantioselective total synthesis of bisdehydroneostemoninine employing L-glutamic acid as t...
The first chapter introduces the reader to the concept of natural product total synthesis and its ...
Total synthesis of natural products with diverse architecture and varying degree of complexity is an...
The isoquinoline alkaloids form a unique class of compounds, exhibiting biological properties almost...
This dissertation features two projects concerning natural product synthesis and reaction developmen...
The planning and implementation of an enantioselective total synthesis of (+)-scholarisine A is pres...
Throughout history, organisms have ensured their survival by producing a wide variety of small molec...