A convergent and enantioselective synthesis of the natural product amurensinine is described. The synthetic strategy takes advantage of mild and selective C−H and C−C bond insertion reactions, in addition to the palladium-catalyzed aerobic oxidative kinetic resolution recently developed in these laboratories
From 2 to 1! Racemic tertiary halooxindoles proceed to enantioenriched oxindoles bearing all-carbon ...
Our efforts toward the construction of the carbocylic core of cortistatin A via an enyne-ene metathe...
Deprotonation of secondary alkane nitriles with nBuLi and addition to aryl imines gives kinetic anti...
The first total syntheses of (−)-trichorabdal A and (−)-longikaurin E are reported. A unified synthe...
An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was exam...
The first enantioselective total synthesis of the epipolythiodiketopiperazine (ETP) natural product ...
A general approach for the synthesis of benzannulated macrolactone natural products utilizing an ary...
The preparation and synthetic applications of benzoquinone monoketal-derived N-tert-butanesulfinyl i...
Cyclic molecular structures are ubiquitous in chemistry. Efficient and convergent methods to synthe...
A synthesis of the C9–C16 segment of ambruticin is described which relies on organoiron methodology ...
Herein we report the first enantioselective total synthesis of (+)-dichroanone, confirming the absol...
We thank the Spanish Ministerio de Ciencia e Innovación (MICINN; grant no. CONSOLIDER INGENIO 2010-C...
Heteroaromatic carboxylic acids have been directly coupled with imines using propylphosphonic anhydr...
The first direct enantioselective organocatalytic intramolecular Diels−Alder reaction has been accom...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
From 2 to 1! Racemic tertiary halooxindoles proceed to enantioenriched oxindoles bearing all-carbon ...
Our efforts toward the construction of the carbocylic core of cortistatin A via an enyne-ene metathe...
Deprotonation of secondary alkane nitriles with nBuLi and addition to aryl imines gives kinetic anti...
The first total syntheses of (−)-trichorabdal A and (−)-longikaurin E are reported. A unified synthe...
An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was exam...
The first enantioselective total synthesis of the epipolythiodiketopiperazine (ETP) natural product ...
A general approach for the synthesis of benzannulated macrolactone natural products utilizing an ary...
The preparation and synthetic applications of benzoquinone monoketal-derived N-tert-butanesulfinyl i...
Cyclic molecular structures are ubiquitous in chemistry. Efficient and convergent methods to synthe...
A synthesis of the C9–C16 segment of ambruticin is described which relies on organoiron methodology ...
Herein we report the first enantioselective total synthesis of (+)-dichroanone, confirming the absol...
We thank the Spanish Ministerio de Ciencia e Innovación (MICINN; grant no. CONSOLIDER INGENIO 2010-C...
Heteroaromatic carboxylic acids have been directly coupled with imines using propylphosphonic anhydr...
The first direct enantioselective organocatalytic intramolecular Diels−Alder reaction has been accom...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
From 2 to 1! Racemic tertiary halooxindoles proceed to enantioenriched oxindoles bearing all-carbon ...
Our efforts toward the construction of the carbocylic core of cortistatin A via an enyne-ene metathe...
Deprotonation of secondary alkane nitriles with nBuLi and addition to aryl imines gives kinetic anti...