Frederick A. Hicks

Affiliations: 
1999 Massachusetts Institute of Technology, Cambridge, MA, United States 
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"Frederick Arthur Hicks"
Bio:

http://hdl.handle.net/1721.1/84738

Mean distance: 7.29
 
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Parents

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Stephen L. Buchwald grad student 1999 MIT
 (The development of titanium-catalyzed enyne cyclocarbonylations and related methodologies)
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Publications

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Demkiw K, Araki H, Elliott EL, et al. (2016) A Nitrogen-assisted One-pot Heteroaryl Ketone Synthesis from Carboxylic Acids and Heteroaryl Halides. The Journal of Organic Chemistry
Armitage I, Elliott EL, Hicks F, et al. (2015) Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat Organic Process Research and Development. 19: 1299-1307
Faul MM, Argentine MD, Egan M, et al. (2015) Part 3: Designation and Justification of API Starting Materials: Proposed Framework for Alignment from an Industry Perspective Organic Process Research and Development. 19: 915-924
Faul MM, Busacca CA, Eriksson MC, et al. (2014) Part 2: Designation and justification of API starting materials: Current practices across member companies of the IQ consortium Organic Process Research and Development. 18: 594-600
Faul MM, Kiesman WF, Smulkowski M, et al. (2014) Part 1: A review and perspective of the regulatory guidance to support designation and justification of API starting material Organic Process Research and Development. 18: 587-593
Buchwald SL, Hicks FA. (2010) ChemInform Abstract: Pauson-Khand-Type Reactions Cheminform. 31: no-no
Hicks FA, Buchwald SL. (2010) ChemInform Abstract: An Intramolecular Titanium-Catalyzed Asymmetric Pauson-Khand Type Reaction. Cheminform. 30: no-no
Hicks FA, Kablaoui NM, Buchwald SL. (2010) ChemInform Abstract: Scope of the Intramolecular Titanocene-Catalyzed Pauson-Khand Type Reaction. Cheminform. 30: no-no
KABLAOUI NM, HICKS FA, BUCHWALD SL. (2010) ChemInform Abstract: Titanocene-Catalyzed Cyclocarbonylation of o-Allyl Aryl Ketones to . gamma.-Butyrolactones. Cheminform. 28: no-no
HICKS FA, BUCHWALD SL. (2010) ChemInform Abstract: Highly Enantioselective Catalytic Pauson-Khand Type Formation of Bicyclic Cyclopentenones. Cheminform. 28: no-no
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