Lista de obras - Brett D Schwartz - Dominio Público Uruguay

A chemoenzymatic and fully stereocontrolled total synthesis of the antibacterial natural product (-)-platencin

artículo científico publicado en 2014

A chemoenzymatic total synthesis of (+)-clividine

artículo científico publicado en 2011

A chemoenzymatic total synthesis of the protoilludane aryl ester (+)-armillarivin

scientific article published on 03 April 2013

A diverse suite of spiroacetals, including a novel branched representative, is released by female Bactrocera tryoni (Queensland fruit fly).

artículo científico publicado en 2006

Asymmetric [4 + 3] cycloadditions between vinylcarbenoids and dienes: application to the total synthesis of the natural product (-)-5-epi-vibsanin E

artículo científico publicado en 2009

End game strategies towards the total synthesis of vibsanin E, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A.

artículo científico publicado en 2008

Metabolomics and genomics combine to unravel the pathway for the presence of fragrance in rice.

artículo científico publicado en 2017

N-Methoxy-N-methylcyanoformamide, a Highly Reactive Reagent for the Formation of β-Keto Weinreb Amides and Unsymmetrical Ketones

scientific article published on 19 July 2016

Oxidative carbon-carbon bond cleavage is a key step in spiroacetal biosynthesis in the fruit fly Bactrocera cacuminata.

artículo científico publicado en 2014

RANEY® cobalt--an underutilised reagent for the selective cleavage of C-X and N-O bonds.

artículo científico publicado en 2014

Rapid and enantioselective assembly of the lycorine framework using chemoenzymatic techniques

artículo científico publicado en 2009

Spiroacetal biosynthesis in fruit flies is complex: distinguishable origins of the same major spiroacetal released by different Bactrocera spp.

artículo científico publicado en 2010

Spiroacetal biosynthesis in insects from Diptera to Hymenoptera: the Giant Ichneumon wasp Megarhyssa nortoni nortoni Cresson.

artículo científico publicado en 2008

Spiroacetal biosynthesis: (+/-)-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (Olive Fruit Fly).

artículo científico publicado en 2005

Structure of the lycorinine alkaloid nobilisitine A

artículo científico publicado el 27 de septiembre de 2011

Synthesis and Antiplasmodial Evaluation of Analogues Based on the Tricyclic Core of Thiaplakortones A-D.

artículo científico publicado en 2015

Synthesis and antimalarial evaluation of amide and urea derivatives based on the thiaplakortone A natural product scaffold

artículo científico publicado en 2015

Synthesis of spirocyclic orthoesters by 'anomalous' rhodium(ii)-catalysed intramolecular C-H insertions

artículo científico publicado en 2017

Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A.

artículo científico publicado en 2010

Synthetic Studies on the Natural Product Myrsinoic Acid F Reveal Biologically Active Analogues

scientific article published on 11 June 2018

Synthetic studies on amaryllidaceae and other terrestrially derived alkaloids.

artículo científico publicado en 2012

Total Synthesis of (±)-Vibsanin E.

artículo científico publicado en 2009

Total Synthesis of the Illicium-Derived Sesquineolignan Simonsol C.

artículo científico publicado en 2016

Total synthesis of thiaplakortone a: derivatives as metabolically stable leads for the treatment of malaria

artículo científico publicado en 2013

Towards the Total Synthesis of 3-Hydroxyvibsanin E.

artículo científico publicado en 2009

Lista de obras de Brett D Schwartz

A chemoenzymatic and fully stereocontrolled total synthesis of the antibacterial natural product (-)-platencin

A chemoenzymatic total synthesis of (+)-clividine

A chemoenzymatic total synthesis of the protoilludane aryl ester (+)-armillarivin

A diverse suite of spiroacetals, including a novel branched representative, is released by female Bactrocera tryoni (Queensland fruit fly).

Asymmetric [4 + 3] cycloadditions between vinylcarbenoids and dienes: application to the total synthesis of the natural product (-)-5-epi-vibsanin E

End game strategies towards the total synthesis of vibsanin E, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A.

Metabolomics and genomics combine to unravel the pathway for the presence of fragrance in rice.

N-Methoxy-N-methylcyanoformamide, a Highly Reactive Reagent for the Formation of β-Keto Weinreb Amides and Unsymmetrical Ketones

Oxidative carbon-carbon bond cleavage is a key step in spiroacetal biosynthesis in the fruit fly Bactrocera cacuminata.

RANEY® cobalt--an underutilised reagent for the selective cleavage of C-X and N-O bonds.

Rapid and enantioselective assembly of the lycorine framework using chemoenzymatic techniques

Spiroacetal biosynthesis in fruit flies is complex: distinguishable origins of the same major spiroacetal released by different Bactrocera spp.

Spiroacetal biosynthesis in insects from Diptera to Hymenoptera: the Giant Ichneumon wasp Megarhyssa nortoni nortoni Cresson.

Spiroacetal biosynthesis: (+/-)-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (Olive Fruit Fly).

Structure of the lycorinine alkaloid nobilisitine A

Synthesis and Antiplasmodial Evaluation of Analogues Based on the Tricyclic Core of Thiaplakortones A-D.

Synthesis and antimalarial evaluation of amide and urea derivatives based on the thiaplakortone A natural product scaffold

Synthesis of spirocyclic orthoesters by 'anomalous' rhodium(ii)-catalysed intramolecular C-H insertions

Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A.

Synthetic Studies on the Natural Product Myrsinoic Acid F Reveal Biologically Active Analogues

Synthetic studies on amaryllidaceae and other terrestrially derived alkaloids.

Total Synthesis of (±)-Vibsanin E.

Total Synthesis of the Illicium-Derived Sesquineolignan Simonsol C.

Total synthesis of thiaplakortone a: derivatives as metabolically stable leads for the treatment of malaria

Towards the Total Synthesis of 3-Hydroxyvibsanin E.