Mark D. McLaws - Concepedia

Author

Mark D. McLaws

University of Utah

Also Known As

M. D. McLaws, Mark D McLaws, Mark D. McLaws, Mark McLaws

Publications

367

Citations

H-Index

Concepts

All Affiliations

University of Utah Albany Molecular Research (United States)

About

Mark D. McLaws is an author at University of Utah specializing in engineering, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	4	4	113
2	Biomolecular Engineering	4	4	73
3	Natural Sciences	3	3	62
4	Biochemistry	2	2	50
5	Medicine	1	1	12

Mark D. McLaws

Publications

258

Citations

H-Index

Page 1

	Year	Citations
A Direct and Mild Conversion of Tertiary Aryl Amides to Methyl Esters Using Trimethyloxonium Tetrafluoroborate: A Very Useful Complement to Directed Metalation Reactions Gary E. Keck, Mark D. McLaws, Travis T. Wager Tetrahedron Chemical EngineeringEngineeringAlkene MetathesisOrganic ChemistryOrganometallic Catalysis	2000	52
Inhibition of chemically-induced neoplastic transformation by a novel tetrasodium diphosphate astaxanthin derivative Laura M. Hix, Dean A. Frey, Mark D. McLaws, Carcinogenesis	2005	46
Asymmetric Total Synthesis of Rhizoxin D Financial support has been provided by the National Institutes of Health (through grant GM-28961) and by Pfizer, Inc. Gary E. Keck, Carrie A. Wager, Travis T. Wager, PubMed Bioorganic ChemistryEngineeringOrganic ChemistryAntimicrobial ChemotherapyChemistry	2001	39
Enantio- and Diastereoselective Additions to Aldehydes Using the Bifunctional Reagent 2-(Chloromethyl)-3-(tributylstannyl)propene: Application to a Synthesis of the C<sub>16</sub>−C<sub>27</sub> Segment of Bryostatin 1 Gary E. Keck, Tao Yu, Mark D. McLaws The Journal of Organic Chemistry	2005	26
Stereoselective synthesis of the C1–C13 segment of dolabelide B Gary E. Keck, Mark D. McLaws Tetrahedron Letters Organic ChemistrySynthetic ChemistryPharmacologyStereoselective Synthesis	2005	24
Initial Process Development and Scale-Up of the Synthesis of a Triple Reuptake Inhibitor ALB 109780 Qiang Yang, Luckner G. Ulysse, Mark D. McLaws, Organic Process Research & Development	2012	21
Process Development and Pilot-Scale Synthesis of New Cyclization Conditions of Substituted Phenylacetamides to Tetrahydroisoquinoline-2-ones Using Eaton’s Reagent Luckner G. Ulysse, Qiang Yang, Mark D. McLaws, Organic Process Research & Development	2009	16
Green Chemistry Articles of Interest to The Pharmaceutical Industry Marian C. Bryan, Andrew Cosbie, Louis J. Diorazio, Organic Process Research & Development Medicinal ChemistryPharmaceutical ChemistryAirport BoulevardDna WayPharmaceutical Science	2017	12
Improved Synthesis of the C16–C20 Segment of Resolvin E1 Using Enantioselective Ketone Reduction and Lipase-Catalyzed Resolution Rasidul Amin, Jian-Xie Chen, Ian C. Cotterill, Organic Process Research & Development EngineeringOrganic ChemistryChemical BiologyLipase-catalyzed ResolutionPharmaceutical Chemistry	2013	11
Semicontinuous Process for GMP Manufacture of a Carbapenem Intermediate via Carbene Insertion Using an Immobilized Rhodium Catalyst James R. Gage, Fu‐Rong Chen, Chang‐Ming Dong, Organic Process Research & Development Chemical EngineeringBiomanufacturingEngineeringCatalytic ApplicationIndustrial Catalysis	2020	11

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