Viresh H. Rawal - Chicago IL, US Yong Huang - Pasadena CA, US Aditya K. Unni - Chicago IL, US Avinash N. Thadani - Chicago IL, US
Assignee:
The University of Chicago - Chicago IL
International Classification:
C07D 315/00 C07C 211/00
US Classification:
549416, 549424, 549419, 564462
Abstract:
Methods of performing cycloadditions are described that include (a) combining a first reactant and a second reactant in a hydrogen bonding solvent to form a reaction mixture; and (b) reacting the first reactant and the second reactant to form a cycloadduct. Methods of performing asymmetric catalytic reactions are also described that include (a) combining a first reactant, a second reactant, and a catalytic amount of a chiral hydrogen-bond donor in a solvent to form a reaction mixture; and (b) reacting the first reactant and the second reactant to form an enantiomeric excess of a reaction product. Reaction mixtures corresponding to these methods are also described.
Methods Of Performing Cycloadditions, Reaction Mixtures, And Methods Of Performing Asymmetric Catalytic Reactions
Viresh H. Rawal - Chicago IL, US Yong Huang - Pasadena CA, US Aditya K. Unni - Chicago IL, US Avinash N. Thadani - Chicago IL, US
Assignee:
The University of Chicago - Chicago IL
International Classification:
C07D 315/00
US Classification:
549416, 549330, 549273, 546 16
Abstract:
Methods of performing cycloadditions are described that include (a) combining a first reactant and a second reactant in a hydrogen bonding solvent to form a reaction mixture; and (b) reacting the first reactant and the second reactant to form a cycloadduct. Methods of performing asymmetric catalytic reactions are also described that include (a) combining a first reactant, a second reactant, and a catalytic amount of a chiral hydrogen-bond donor in a solvent to form a reaction mixture; and (b) reacting the first reactant and the second reactant to form an enantiomeric excess of a reaction product. Reaction mixtures corresponding to these methods are also described.
- San Diego CA, US Aditya Krishnan Unni - San Diego CA, US Yosef Shamay - San Diego CA, US Kevin Duane Bunker - Escondido CA, US Peter Qinhua Huang - San Diego CA, US
International Classification:
A61K 31/5377 A61K 31/496 A61K 9/51 A61K 47/64
Abstract:
Various albumin nanoparticle Bcl-2 inhibitor formulations are described, along with methods of using them to treat conditions characterized by excessive cellular proliferation, such as cancer and tumors. In various embodiments, such Bcl-2 inhibitor formulations contain albumin and a compound of the following Formula (I), or a pharmaceutically acceptable salt thereof, where the variables in Formula (I) are defined herein.
- San Diego CA, US Brant Clayton Boren - San Diego CA, US Sobhana Babu Boga - San Diego CA, US Aditya Krishnan Unni - San Diego CA, US Peter Qinhua Huang - San Diego CA, US Kevin Duane Bunker - Escondido CA, US Benjamin Anthony Pratt - Encinitas CA, US
International Classification:
C07F 9/59 C07F 9/572
Abstract:
Disclosed herein are methods for preparing tertiary alcohols from an optionally substituted phenyl ketone or an optionally substituted pyridinyl ketone that includes the use of a chiral ligand and boron trifluoride diethyl etherate. Tertiary alcohols can be used to prepare synthetic versions of natural products and/or pharmaceuticals.
- San Diego CA, US Kevin Duane Bunker - Escondido CA, US Brant Clayton Boren - San Diego CA, US Sayee Gajanan Hegde - San Diego CA, US Hui Liu - San Diego CA, US Aditya Krishnan Unni - San Diego CA, US Sunny Abraham - San Diego CA, US Chad Daniel Hopkins - San Diego CA, US Sunil Paliwal - Monroe Township NJ, US
International Classification:
C07D 487/04 C07D 491/048
Abstract:
Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.
Illinois Institute of Technology since Aug 2009
Assistant Professor
Rockhurst University Aug 2008 - May 2009
Visiting Assistant Professor
University of Tokyo Jun 2005 - Jun 2007
J.S.P.S. post-doctoral research fellow
University of Chicago 1998 - 2005
Graduate Student
Mayo Clinic, Department of Laboratory Medicine and Pathology 1995 - 1998
Clinical Chemist
Education:
University of Chicago 1998 - 2005
Ph.D., Chemistry
St. Olaf College 1990 - 1994
B.A., Chemistry
Skills:
Synthetic Organic Chemistry Asymmetric Catalysis Homogeneous Catalysis Small Molecules Catalysis Materials Science Higher Education Organic Chemistry Organic Synthesis Spectroscopy Medicinal Chemistry Drug Discovery Nanoparticle Drug Delivery Total Synthesis Organocatalysis
Assistant Professor at Illinois Institute of Technology
Location:
Greater Chicago Area
Industry:
Research
Work:
Illinois Institute of Technology since Aug 2009
Assistant Professor
Rockhurst University Aug 2008 - May 2009
Visiting Assistant Professor
University of Tokyo Jun 2005 - Jun 2007
J.S.P.S. post-doctoral research fellow
University of Chicago 1998 - 2005
Graduate Student
Mayo Clinic, Department of Laboratory Medicine and Pathology 1995 - 1998
Clinical Chemist
Education:
University of Chicago 1998 - 2005
Ph.D., Chemistry
St. Olaf College 1990 - 1994
B.A., Chemistry
Honor & Awards:
Japan Society for the Promotion of Science Post-doctoral Research Fellowship
Division of Physcal Sciences Teaching Prize, University of Chicago
GAANN Pre-doctoral fellowship
Departmental Distinction, St. Olaf College
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