Add to ORKGImage Persented A facile route to enantiomerically pure (+)-nootkatone and derivatives has been established through conjunctive stereoselective Grignard/anionic oxy-Cope (AOC) reactions. © 2009 American Chemical Society
Since around the turn of the millennium, organocatalysis developed rapidly and have been seen as one...
International audiencePolycyclic structures fused at a central carbon are of great interest due to t...
A short asymmetric synthesis of (R)-(+)-Goniothalamin oxide was developed and synthesized using a Le...
Research, inspired by nature, provides ample opportunity for discovery, ingenuity, and creative ende...
An efficient enantioselective synthesis of lactones was developed based on the catalytic asymmetric ...
A racemic synthesis of azanoradamantane (±)-3 was accomplished via Yamamoto\u27s MAD-catalyzed Diels...
The C11–C17 segment of the antifungal agent soraphen A1α was prepared from glyceraldehyde acetonide ...
Direct syntheses of 7,8-dihydroxycalamenene and mansonone C were achieved. The cis-stereochemistry r...
Both isomers of naphthotectone, an isoprenoid quinone from Verbenaceae Tectona grandis possessing in...
A feasible and enantioselective total synthesis of (−)-trans-dihydronarciclasine [(−)-1], a highly b...
Herein, we report the synthesis of the enantiomers of trinorbornane, a tetracyclic saturated hydroca...
Recent advancement in the area of asymmetric organocatalysis led to the development of new methodolo...
A stable aminal formed stereoselectively from (R,R)-N-tosyl-1,2-diphenyl-1,2-ethylenediamine (TsDPEN...
Described in this report is an enantioselective route toward the chamigrene natural product family. ...
We present a four-step synthesis of (+)-artemone from (–)- linalool, featuring iminium organocatalys...
Since around the turn of the millennium, organocatalysis developed rapidly and have been seen as one...
International audiencePolycyclic structures fused at a central carbon are of great interest due to t...
A short asymmetric synthesis of (R)-(+)-Goniothalamin oxide was developed and synthesized using a Le...
Research, inspired by nature, provides ample opportunity for discovery, ingenuity, and creative ende...
An efficient enantioselective synthesis of lactones was developed based on the catalytic asymmetric ...
A racemic synthesis of azanoradamantane (±)-3 was accomplished via Yamamoto\u27s MAD-catalyzed Diels...
The C11–C17 segment of the antifungal agent soraphen A1α was prepared from glyceraldehyde acetonide ...
Direct syntheses of 7,8-dihydroxycalamenene and mansonone C were achieved. The cis-stereochemistry r...
Both isomers of naphthotectone, an isoprenoid quinone from Verbenaceae Tectona grandis possessing in...
A feasible and enantioselective total synthesis of (−)-trans-dihydronarciclasine [(−)-1], a highly b...
Herein, we report the synthesis of the enantiomers of trinorbornane, a tetracyclic saturated hydroca...
Recent advancement in the area of asymmetric organocatalysis led to the development of new methodolo...
A stable aminal formed stereoselectively from (R,R)-N-tosyl-1,2-diphenyl-1,2-ethylenediamine (TsDPEN...
Described in this report is an enantioselective route toward the chamigrene natural product family. ...
We present a four-step synthesis of (+)-artemone from (–)- linalool, featuring iminium organocatalys...
Since around the turn of the millennium, organocatalysis developed rapidly and have been seen as one...
International audiencePolycyclic structures fused at a central carbon are of great interest due to t...
A short asymmetric synthesis of (R)-(+)-Goniothalamin oxide was developed and synthesized using a Le...