D. J. Wallace

发表

The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the CD-spiroacetal segment.

K. Gibson, I. Paterson, M. J. Coster, 2005, Organic & biomolecular chemistry.

Process Development and Multikilogram-Scale Synthesis of a TRPV1 Antagonist

Jeremy P. Scott, D. J. Wallace, Faye J. Sheen, 2013 .

Enantioselective Synthesis of a Highly Substituted Tetrahydrofluorene Derivative as a Potent and Selective Estrogen Receptor Beta Agonist

Jeremy P. Scott, Matthew L. Maddess, J. Lynch, 2014 .

Development of a Fit-for-Purpose Large-Scale Synthesis of an Oral PARP Inhibitor

Daniel J. Muzzio, Paul Fernandez, P. Sajonz, 2011 .

Discovery and Chemical Development of Suvorexant - A Dual Orexin Antagonist for Sleep Disorder

P. Coleman, I. Mangion, D. J. Wallace, 2016 .

Exploiting catalyst characteristics: A protocol for increasing diastereoselectivity in a double ring-closing metathesis reaction

D. J. Wallace, 2006 .

Copper-mediated reaction of 2-halopyridines with ethyl bromodifluoroacetate

D. J. Wallace, Cameron J. Cowden, A. Davies, 2002 .

Use of Commercially Available Ruthenium Fischer-Type Carbenes for Ring-Closing Metathesis Reactions: Scope and Limitations of an in situ Activation Procedure

D. J. Wallace, 2009 .

On the mechanism of a double ring-closing metathesis reaction

D. J. Wallace, 2005 .

Observations on the DDQ Oxidation of 1-Acyldihydropyridines - A Synthetic Application

D. J. Wallace, Andrew D. Gibb, K. Brands, 2001 .

New Efficient Asymmetric Synthesis of Taranabant, a CB1R Inverse Agonist for the Treatment of Obesity

D. Zewge, Yong-kui Sun, Cheng-yi Chen, 2009 .

Palladium-catalyzed amidation of enol triflates: a new synthesis of enamides.

David J. Klauber, R. Volante, Cheng-yi Chen, 2003, Organic letters.

Reaction development and mechanistic study of a ruthenium catalyzed intramolecular asymmetric reductive amination en route to the dual Orexin inhibitor Suvorexant (MK-4305).

Timothy J. Wright, R. Reamer, S. Krska, 2011, Journal of the American Chemical Society.

Relay ring-closing metathesis-a strategy for achieving reactivity and selectivity in metathesis chemistry.

D. J. Wallace, 2005, Angewandte Chemie.

Phosphine-catalyzed cycloadditions of allenic ketones: new substrates for nucleophilic catalysis.

R. Reamer, D. J. Wallace, Rachel L. Sidda, 2007, The Journal of organic chemistry.

New synthesis of a selective estrogen receptor modulator using an enatioselective phosphine-mediated 2+3 cycloaddition

R. Reamer, D. J. Wallace, 2013 .

Stereoselective Double Ring Closing Metathesis Reactions in the Synthesis of Spirocyclic Compounds.

P. Bulger, D. J. Wallace, U. Dolling, 2000 .

Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1.

A. P. Hodgson, R. Oballa, K. Gibson, 2001, Angewandte Chemie.

Studies in polypropionate synthesis: High π-face selectivity in syn and anti aldol reactions of chiral boron enolates of lactate-derived ketones

I. Paterson, D. J. Wallace, Silvia M. Velázquez, 1994 .

Practical synthesis of a highly functionalized thiazole ketone

L. Tan, E. Grabowski, Cheng-yi Chen, 2003 .

Total synthesis of (−)-hemiasterlin, a structurally novel tripeptide that exhibits potent cytotoxic activity

R. Andersen, John Coleman, D. J. Wallace, 1997 .

Manipulation of the aldol adducts from lactate-derived ketones. A versatile chiral auxiliary for the asymmetric synthesis of β-hydroxy carbonyl compounds

I. Paterson, D. J. Wallace, 1994 .

Stereoselective Aldol Reactions in the Synthesis of Polyketide Natural Products

I. Paterson, D. J. Wallace, Cameron J. Cowden, 2007 .

Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1.

A. P. Hodgson, R. Oballa, K. Gibson, 2001, Angewandte Chemie.

Cyclopropylboronic acid: synthesis and Suzuki cross-coupling reactions

Cheng-yi Chen, D. J. Wallace, 2002 .

Stereocontrolled, Two-Directional, Chain Synthesis Using the Boron Aldol Reaction and Double Ireland-Claisen Rearrangement.

I. Paterson, A. Hulme, D. J. Wallace, 1991 .

Studies in marine macrolide synthesis: Synthesis of a C16C28 subunit of spongistatin 1 (altohyrtin A) incorporating the CD-spiroacetal moiety

K. Gibson, I. Paterson, D. J. Wallace, 1997 .

Synthesis of Cytotoxic Marine Macrolides: An Aldol-Based Approach to Spongistatin 1 (Altohyrtin A)

R. Oballa, K. Gibson, I. Paterson, 1999 .

A double ring closing metathesis reaction in the rapid, enantioselective synthesis of NK-1 receptor antagonists.

J. Goodman, P. Reider, D. J. Wallace, 2001, Organic letters.

The First Large-Scale Synthesis of MK-4305: A Dual Orexin Receptor Antagonist for the Treatment of Sleep Disorder

R. Reamer, D. J. Wallace, Faye J. Sheen, 2011 .

Convergent, Kilogram Scale Synthesis of an Akt Kinase Inhibitor

Daniel J. Muzzio, L. Tan, Dalian Zhao, 2012 .

Development of a Phase Transfer Catalyzed Asymmetric Synthesis for an Estrogen Receptor Beta Selective Agonist

Jeremy P. Scott, S. Oliver, Khateeta M. Emerson, 2008 .

An investigation into causes and effects of high cyanide levels in the palladium-catalyzed cyanation reaction.

Y. Liu, Yadan W. Chen, Jeff Strine, 2004, Organic letters.

Accelerated Development of a Scalable Synthesis of CY6463, a CNS-Penetrant sGC Stimulator for the Treatment of Neurodegenerative Diseases

D. J. Wallace, William S. Kissel, Anna Balanov, 2021, Organic Process Research & Development.

CB1R Inverse Agonist – Taranabant

D. J. Wallace, 2010 .

Relay Ring-Closing Metathesis — A Strategy for Achieving Reactivity and Selectivity in Metathesis Chemistry

D. J. Wallace, 2005 .

CRTH2 antagonist MK-7246: a synthetic evolution from discovery through development.

Stephen Lau, Danny Gauvreau, D. Gauvreau, 2012, The Journal of organic chemistry.

Synthesis and antimitotic/cytotoxic activity of hemiasterlin analogues.

R. Andersen, J. Nieman, M. Roberge, 2003, Journal of natural products.

Ring-closing metathesis reactions of bis(enynes): selectivity and surprises.

R. Reamer, D. J. Wallace, 2014, The Journal of organic chemistry.

The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation.

I. Paterson, M. J. Coster, J. L. Aceña, 2005, Organic & biomolecular chemistry.

Modified flotation technique for quantitative determination of mite populations in feedstuffs.

B. Thind, D. J. Wallace, 1984, Journal - Association of Official Analytical Chemists.

Transition Metal‐Catalyzed Coupling Reactions in the Synthesis of Taranabant: from Inception to Pilot Implementation

D. J. Wallace, 2013 .

Process Development and Large-Scale Synthesis of a c-Met Kinase Inhibitor

Simon E. Hamilton, Jeremy P. Scott, D. J. Wallace, 2010 .

Development of a Practical Manufacturing Process to Relebactam via Thorough Understanding of the Origin and Control of Oligomeric Impurities

T. Itoh, Feiyue Wu, B. Sherry, 2021, Organic Process Research & Development.

Catalytic, Enantioselective Synthesis of Taranabant, a Novel, Acyclic Cannabinoid-1 Receptor Inverse Agonist for the Treatment of Obesity

Alex M. Chen, Jeff Strine, Cheng-yi Chen, 2007 .

A quadruple ring-closing metathesis reaction in the synthesis of bis-spirocyclic compounds: extending the scope of metathesis chemistry

D. J. Wallace, 2003 .