S. M. Dalby

发表

Total Synthesis of the Antimitotic Marine Macrolide (−)-Leiodermatolide

I. Paterson, K. Ng, Simon R Williams, 2014, Angewandte Chemie.

The stereocontrolled total synthesis of spirastrellolide A methyl ester. Fragment coupling studies and completion of the synthesis.

E. Anderson, I. Paterson, S. M. Dalby, 2012, Organic & biomolecular chemistry.

The stereocontrolled total synthesis of spirastrellolide A methyl ester. Expedient construction of the key fragments.

E. Anderson, I. Paterson, O. Loiseleur, 2012, Organic & biomolecular chemistry.

Strategy Evolution in the Total Synthesis of Spirastrellolide A Methyl Ester

I. Paterson, S. M. Dalby, P. Maltas, 2011 .

Synthesis and stereochemical determination of the spirastrellolides.

I. Paterson, S. M. Dalby, 2009, Natural product reports.

Total synthesis of spirastrellolide A methyl ester--part 1: Synthesis of an advanced C17-C40 bis-spiroacetal subunit.

E. Anderson, I. Paterson, Julien Genovino, 2008, Angewandte Chemie.

Synthesis of two diastereomeric C1-C22 fragments of spirastrellolide A.

E. Anderson, I. Paterson, Julien Genovino, 2007, Chemical communications.

Synthesis of the DEF-bis-spiroacetal of spirastrellolide A exploiting a double asymmetric dihydroxylation/spiroacetalisation strategy.

E. Anderson, I. Paterson, S. M. Dalby, 2006, Chemical communications.

Total synthesis of spirastrellolide A methyl ester--part 2: Subunit union and completion of the synthesis.

E. Anderson, I. Paterson, Julien Genovino, 2008, Angewandte Chemie.

From nature to the laboratory and into the clinic.

K. Nicolaou, Jason S. Chen, S. M. Dalby, 2009, Bioorganic & medicinal chemistry.

Manufacturing Process Development for Belzutifan, Part 3: Completing a Streamlined Through-Process with a Safe and Scalable Oxidation

S. M. Dalby, Jungchul Kim, Feng Peng, 2021, Organic Process Research & Development.

Manufacturing Process Development for Belzutifan, Part 4: Nitrogen Flow Criticality for Transfer Hydrogenation Control

S. M. Dalby, Brittany M. Armstrong, Zachary E. X. Dance, 2021, Organic Process Research & Development.

Kilogram-Scale Synthesis of 2′-C-Methyl-arabino-Uridine from Uridine via Dynamic Selective Dipivaloylation

Timothy J. Wright, Tyler A. Davis, Louis-Charles Campeau, 2021, Organic Process Research & Development.

Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods†

Timothy J. Wright, Rebecca T. Ruck, Tyler A. Davis, 2021, Chemical science.

Asymmetric Synthesis of Letermovir Using a Novel Phase-Transfer-Catalyzed Aza-Michael Reaction

G. Humphrey, S. M. Dalby, Z. Song, 2016 .

Total synthesis of (-)-rhizopodin.

I. Paterson, S. M. Dalby, J. Goodwin-Tindall, 2012, Angewandte Chemie.

Synthesis of the macrocyclic core of leiodermatolide.

I. Paterson, S. M. Dalby, Tanya Paquet, 2011, Organic Letters.

Strategy Evolution in the Total Synthesis of Spirastrellolide A Methyl Ester

I. Paterson, S. M. Dalby, P. Maltas, 2011 .

Manufacturing Process Development for Belzutifan, Part 1: A Concise Synthesis of the Indanone Starting Material

Q. Xiang, L. Tan, G. Gong, 2021, Organic Process Research & Development.

An Investigation into the Unexpected Corrosion of Nickel Alloy Vessels with Selectfluor

Donald C. Bachert, S. M. Dalby, Tao Wang, 2021, Organic Process Research & Development.

Manufacturing Process Development for Belzutifan, Part 5: A Streamlined Fluorination–Dynamic Kinetic Resolution Process

E. Sirota, S. Axnanda, M. Weisel, 2021, Organic Process Research & Development.

Total synthesis of (+)-azinothricin and (+)-kettapeptin.

K. Hale, S. Manaviazar, S. M. Dalby, 2009, Organic letters.

A concise asymmetric total synthesis of aspidophytine.

K. Nicolaou, S. M. Dalby, U. Majumder, 2008, Journal of the American Chemical Society.

Toward the synthesis of spirastrellolide A: construction of two C1-C25 diastereomers containing the BC-spiroacetal.

E. Anderson, I. Paterson, O. Loiseleur, 2005, Organic letters.

Toward the synthesis of spirastrellolide a: construction of a tetracyclic C26-C40 subunit containing the DEF-bis-spiroacetal.

E. Anderson, I. Paterson, O. Loiseleur, 2005, Organic letters.

A second-generation total synthesis of spirastrellolide A methyl ester.

E. Anderson, I. Paterson, S. M. Dalby, 2012, Angewandte Chemie.

Total Synthesis of Jiadifenolide**

I. Paterson, S. M. Dalby, Meng Xuan, 2014, Angewandte Chemie.

Total synthesis of (+)-haplophytine.

K. Nicolaou, Takahiro Suzuki, D. Y. Chen, 2009, Angewandte Chemie.

Manufacturing Process Development for Belzutifan, Part 6: Ensuring Scalability for a Deoxyfluorination Reaction

Timothy J. Wright, David J. Lamberto, J. McMullen, 2021, Organic Process Research & Development.

Total synthesis of alotaketal A.

I. Paterson, S. M. Dalby, Meng Xuan, 2012, Organic letters.

Synthesis of the C1-C21 Southern Hemisphere of the Originally Proposed Structure of Spirastrellolide A

E. Anderson, I. Paterson, S. M. Dalby, 2005 .

Synthesis of polyketide natural products and analogs as promising anticancer agents.

I. Paterson, S. M. Dalby, 2011, Current opinion in drug discovery & development.

Synthesis of Spirastrellolide A Methyl Ester

E. Anderson, I. Paterson, Julien Genovino, 2008 .

Progress toward a total synthesis of spirastrellolide A

E. Anderson, I. Paterson, O. Loiseleur, 2007 .

Leiodermatolide, a potent antimitotic macrolide from the marine sponge Leiodermatium sp.

R. Isbrucker, D. Divlianska, A. Wright, 2011, Angewandte Chemie.

Benzylic Photobromination for the Synthesis of Belzutifan: Elucidation of Reaction Mechanisms Using In Situ LED-NMR.

J. McMullen, F. Lévesque, Karthik Narsimhan, 2021, The Journal of organic chemistry.

Manufacturing Process Development for Belzutifan, Part 2: A Continuous Flow Visible-Light-Induced Benzylic Bromination

J. McMullen, L. Tan, M. Wismer, 2021, Organic Process Research & Development.