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Solution−Liquid−Solid (SLS) Growth of Silicon Nanowires

Journal of the American Chemical Society, 2008-04, Vol.130 (16), p.5436-5437

2008

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Lamellar Twinning in Semiconductor Nanowires

Journal of physical chemistry. C, 2007-02, Vol.111 (7), p.2929-2935

2007

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Twin-Related Branching of Solution-Grown ZnSe Nanowires

Chemistry of materials, 2007-10, Vol.19 (20), p.4943-4948

2007

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Bismuth Nanocrystal-Seeded III-V Semiconductor Nanowire Synthesis

Crystal growth & design, 2005-09, Vol.5 (5), p.1971-1976

2005

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ZnE (E = S, Se, Te) Nanowires Grown by the Solution−Liquid−Solid Mechanism: Importance of Reactant Decomposition Kinetics and the Solvent

Crystal growth & design, 2008-09, Vol.8 (9), p.3246-3252

2008

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Preparation of the HIV Attachment Inhibitor BMS-663068. Part 7. Development of a Regioselective Ullmann–Goldberg–Buchwald Reaction

Organic process research & development, 2017-08, Vol.21 (8), p.1156-1165

2017

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High Yield Solution−Liquid−Solid Synthesis of Germanium Nanowires

Journal of the American Chemical Society, 2005-11, Vol.127 (45), p.15718-15719

2005

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Preparation of the HIV Attachment Inhibitor BMS-663068. Part 1. Evolution of Enabling Strategies

Organic process research & development, 2017-08, Vol.21 (8), p.1095-1109

2017

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A Method for Heteroaromatic Nitration Demonstrating Remarkable Thermal Stability

Organic process research & development, 2014-12, Vol.18 (12), p.1812-1820

2014

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Enabling technologies for process intensification in pharmaceutical research and manufacturing

Current opinion in chemical engineering, 2023-09, Vol.41, p.100920, Article 100920

2023

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C–H Arylation in the Formation of a Complex Pyrrolopyridine, the Commercial Synthesis of the Potent JAK2 Inhibitor, BMS-911543

Journal of organic chemistry, 2019-04, Vol.84 (8), p.4661-4669

2019

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Rapid Development of a Commercial Process for Linrodostat, an Indoleamine 2,3-Dioxygenase (IDO) Inhibitor

Organic process research & development, 2019-11, Vol.23 (11), p.2482-2498

2019

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Synthesis of the 6‑Azaindole Containing HIV‑1 Attachment Inhibitor Pro-Drug, BMS-663068

Journal of organic chemistry, 2014-09, Vol.79 (18), p.8757-8767

2014

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Preparation of the HIV Attachment Inhibitor BMS-663068. Part 5. Selective C‑7 Bromination of the 6‑Azaindole Core

Organic process research & development, 2017-08, Vol.21 (8), p.1137-1144

2017

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Preparation of the HIV Attachment Inhibitor BMS-663068. Part 3. Mechanistic Studies Enable a Scale-Independent Friedel–Crafts Acylation

Organic process research & development, 2017-08, Vol.21 (8), p.1122-1130

2017

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Development of a scalable palladium-catalyzed α-arylation process for the synthesis of a CGRP antagonist

Tetrahedron, 2013-07, Vol.69 (27-28), p.5677-5684

2013

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Preparation of the HIV Attachment Inhibitor BMS-663068. Part 4. Synthesis of the 6‑Azaindole Core

Organic process research & development, 2017-08, Vol.21 (8), p.1131-1136

2017

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Preparation of the HIV Attachment Inhibitor BMS-663068. Part 9. Active Pharmaceutical Ingredient Process Development and Powder Properties

Organic process research & development, 2017-08, Vol.21 (8), p.1174-1185

2017

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Solution phase synthesis and characterization of III-V, II-VI and cadmium selenium telluride semiconductor nanowires

Fanfair, Dayne Dustan

2008

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Solution−Liquid−Solid (SLS) Growth of Silicon Nanowires

Lamellar Twinning in Semiconductor Nanowires

Twin-Related Branching of Solution-Grown ZnSe Nanowires

Bismuth Nanocrystal-Seeded III-V Semiconductor Nanowire Synthesis

ZnE (E = S, Se, Te) Nanowires Grown by the Solution−Liquid−Solid Mechanism: Importance of Reactant Decomposition Kinetics and the Solvent

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 7. Development of a Regioselective Ullmann–Goldberg–Buchwald Reaction

High Yield Solution−Liquid−Solid Synthesis of Germanium Nanowires

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 1. Evolution of Enabling Strategies

A Method for Heteroaromatic Nitration Demonstrating Remarkable Thermal Stability

Enabling technologies for process intensification in pharmaceutical research and manufacturing

C–H Arylation in the Formation of a Complex Pyrrolopyridine, the Commercial Synthesis of the Potent JAK2 Inhibitor, BMS-911543

Rapid Development of a Commercial Process for Linrodostat, an Indoleamine 2,3-Dioxygenase (IDO) Inhibitor

Synthesis of the 6‑Azaindole Containing HIV‑1 Attachment Inhibitor Pro-Drug, BMS-663068

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 5. Selective C‑7 Bromination of the 6‑Azaindole Core

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 3. Mechanistic Studies Enable a Scale-Independent Friedel–Crafts Acylation

Development of a scalable palladium-catalyzed α-arylation process for the synthesis of a CGRP antagonist

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 4. Synthesis of the 6‑Azaindole Core

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 9. Active Pharmaceutical Ingredient Process Development and Powder Properties

Solution phase synthesis and characterization of III-V, II-VI and cadmium selenium telluride semiconductor nanowires

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