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Stereospecific Formal Total Synthesis of Ecteinascidin 743

Angewandte Chemie (International ed.), 2006-03, Vol.45 (11), p.1754-1759

2006

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Sixteen-Membered Macrolides: Chemical Modifications and Future Applications

Heterocycles, 2014-02, Vol.89 (2), p.281

2014

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In vitro and in vivo activities of the diazabicyclooctane OP0595 against AmpC-derepressed Pseudomonas aeruginosa

Journal of antibiotics, 2017-03, Vol.70 (3), p.246-250

2017

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Total Synthesis of Cribrostatin IV: Fine-Tuning the Character of an Amide Bond by Remote Control

Journal of the American Chemical Society, 2005-04, Vol.127 (13), p.4596-4598

2005

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OP0595, a new diazabicyclooctane: mode of action as a serine β-lactamase inhibitor, antibiotic and β-lactam 'enhancer'

Journal of antimicrobial chemotherapy, 2015-10, Vol.70 (10), p.2779-2786

2015

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In Vitro and In Vivo Activities of OP0595, a New Diazabicyclooctane, against CTX-M-15-Positive Escherichia coli and KPC-Positive Klebsiella pneumoniae

Antimicrobial agents and chemotherapy, 2016-05, Vol.60 (5), p.3001-3006

2016

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Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position: I. Epimerization and Methylation of the 3-Hydroxyl Group

The Journal of Antibiotics, 2003/04/25, Vol.56(4), pp.399-414

2003

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OP0595, a new diazabicyclooctane: mode of action as a serine [Beta]-lactamase inhibitor, antibiotic and [Beta]-lactam 'enhancer'

Journal of antimicrobial chemotherapy, 2015-10, Vol.70 (10), p.2779

2015

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Synthesis and structure–activity relationships of N-aryl-piperidine derivatives as potent (partial) agonists for human histamine H3 receptor

Bioorganic & medicinal chemistry, 2010-07, Vol.18 (14), p.5441-5448

2010

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Synthesis and determination of the absolute configuration of fudecalone

ARKIVOC, 2003-11, Vol.2003 (8), p.267-282

2003

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Design and synthesis of novel leucomycin analogues modified at the C-3 position. Part II: 3- O-(3-Aryl-2-propenyl)leucomycin analogues

Bioorganic & medicinal chemistry, 2008-04, Vol.16 (8), p.4401-4418

2008

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Novel 16-membered macrolides modified at C-12 and C-13 positions of midecamycin A1 and miokamycin. Part 1. Synthesis and evaluation of 12,13-carbamate and 12-arylalkylamino-13-hydroxy analogues

Bioorganic & medicinal chemistry, 2008-04, Vol.16 (7), p.3985-4002

2008

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Novel 16-membered macrolides modified at C-12 and C-13 positions of midecamycin A 1 and miokamycin. Part 1: Synthesis and evaluation of 12,13-carbamate and 12-arylalkylamino-13-hydroxy analogues

Bioorganic & medicinal chemistry, 2008, Vol.16 (7), p.3985-4002

2008

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Design and synthesis of novel leucomycin analogues modified at the C-3 position. Part II. 3-0-(3-Aryl-2-propenyl)leucomycin analogues

Bioorganic & medicinal chemistry, 2008, Vol.16 (8), p.4401-4418

2008

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Synthesis and revision of the relative configuration of fudecalone

Tetrahedron letters, 2001-01, Vol.42 (5), p.917-919

2001

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Stereospecific Formal Total Synthesis of Ecteinascidin 743

Angewandte Chemie, 2006-03, Vol.118 (11), p.1786-1791

2006

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Total Synthesis of Cribrostatin IV: Fine-Tuning the Character of an Amide Bond by Remote Control [J. Am. Chem. Soc. 2005, 127, 4596−4598].

Journal of the American Chemical Society, 2005-05, Vol.127 (19), p.7262-7262

2005

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Synthesis of the Proposed Structure of Fudecalone, an Anticoccidial Drimane Terpenoid

Organic letters, 1999-10, Vol.1 (7), p.1079-1080

1999

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ChemInform Abstract: Sixteen-Membered Macrolides: Chemical Modifications and Future Applications

ChemInform, 2014-04, Vol.45 (13), p.no-no

2014

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Stereospecific Formal Total Synthesis of Ecteinascidin 743

Angewandte Chemie, 2006-03, Vol.118 (11), p.1786-1791

2006

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Pheromone Synthesis, CLXV. A New Synthesis of (3S,7R,8E,10E)-3,7,9-Trimethyl-8,10-dodecadien-6-one, the Major Component of the Sex Pheromone of the Maritime Pine Scale

Liebigs Annalen der Chemie, 1994-09, Vol.1994 (10), p.971-974

1994

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Pheromone synthesis, CLXXI. A new synthesis of (2E,4E,6R10R)-4,6,10,12-tetramethyl-2,4-tridecadien-7-one (matsuone), the primary component of the sex pheromone of three Matsucoccus pine bast scales

Liebigs Annalen, 1995-12, Vol.1995 (12), p.2093-2099

1995

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Stereospecific Formal Total Synthesis of Ecteinascidin 743

ChemInform, 2006-07, Vol.37 (27), p.no-no

2006

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Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position. Part 1. Epimerization and Methylation of the 3-Hydroxyl Group

ChemInform, 2003-10, Vol.34 (42), p.no-no

2003

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Iterative method for phase extraction from phase-shifting interferograms with spatial noise

Results in optics, 2021-12, Vol.5, p.100192, Article 100192

2021

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Stereospecific Formal Total Synthesis of Ecteinascidin 743

Sixteen-Membered Macrolides: Chemical Modifications and Future Applications

In vitro and in vivo activities of the diazabicyclooctane OP0595 against AmpC-derepressed Pseudomonas aeruginosa

Total Synthesis of Cribrostatin IV: Fine-Tuning the Character of an Amide Bond by Remote Control

OP0595, a new diazabicyclooctane: mode of action as a serine β-lactamase inhibitor, antibiotic and β-lactam 'enhancer'

In Vitro and In Vivo Activities of OP0595, a New Diazabicyclooctane, against CTX-M-15-Positive Escherichia coli and KPC-Positive Klebsiella pneumoniae

Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position: I. Epimerization and Methylation of the 3-Hydroxyl Group

OP0595, a new diazabicyclooctane: mode of action as a serine [Beta]-lactamase inhibitor, antibiotic and [Beta]-lactam 'enhancer'

Synthesis and structure–activity relationships of N-aryl-piperidine derivatives as potent (partial) agonists for human histamine H3 receptor

Synthesis and determination of the absolute configuration of fudecalone

Design and synthesis of novel leucomycin analogues modified at the C-3 position. Part II: 3- O-(3-Aryl-2-propenyl)leucomycin analogues

Novel 16-membered macrolides modified at C-12 and C-13 positions of midecamycin A1 and miokamycin. Part 1. Synthesis and evaluation of 12,13-carbamate and 12-arylalkylamino-13-hydroxy analogues

Novel 16-membered macrolides modified at C-12 and C-13 positions of midecamycin A 1 and miokamycin. Part 1: Synthesis and evaluation of 12,13-carbamate and 12-arylalkylamino-13-hydroxy analogues

Design and synthesis of novel leucomycin analogues modified at the C-3 position. Part II. 3-0-(3-Aryl-2-propenyl)leucomycin analogues

Synthesis and revision of the relative configuration of fudecalone

Stereospecific Formal Total Synthesis of Ecteinascidin 743

Total Synthesis of Cribrostatin IV: Fine-Tuning the Character of an Amide Bond by Remote Control [J. Am. Chem. Soc. 2005, 127, 4596−4598].

Synthesis of the Proposed Structure of Fudecalone, an Anticoccidial Drimane Terpenoid

ChemInform Abstract: Sixteen-Membered Macrolides: Chemical Modifications and Future Applications

Stereospecific Formal Total Synthesis of Ecteinascidin 743

Pheromone Synthesis, CLXV. A New Synthesis of (3S,7R,8E,10E)-3,7,9-Trimethyl-8,10-dodecadien-6-one, the Major Component of the Sex Pheromone of the Maritime Pine Scale

Pheromone synthesis, CLXXI. A new synthesis of (2E,4E,6R10R)-4,6,10,12-tetramethyl-2,4-tridecadien-7-one (matsuone), the primary component of the sex pheromone of three Matsucoccus pine bast scales

Stereospecific Formal Total Synthesis of Ecteinascidin 743

Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position. Part 1. Epimerization and Methylation of the 3-Hydroxyl Group

Iterative method for phase extraction from phase-shifting interferograms with spatial noise

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