Miao Yu, Ph.D.

Affiliations: 
2014 GSAS - Chemistry Boston College, Newton, MA, United States 
Area:
catalysts
Google:
"Miao Yu"
Mean distance: 8.07
 
SNBCP

Parents

Sign in to add mentor
Amir H. Hoveyda grad student 2014 Boston College
 (Stereoselective olefin metathesis reactions for natural product synthesis.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Dockendorff C, Faloon PW, Yu M, et al. (2015) Indolinyl-Thiazole Based Inhibitors of Scavenger Receptor-BI (SR-BI)-Mediated Lipid Transport. Acs Medicinal Chemistry Letters. 6: 375-380
Dockendorff C, Faloon PW, Germain A, et al. (2015) Discovery of bisamide-heterocycles as inhibitors of scavenger receptor BI (SR-BI)-mediated lipid uptake. Bioorganic & Medicinal Chemistry Letters. 25: 2594-8
Dockendorff C, Faloon PW, Pu J, et al. (2015) Benzo-fused lactams from a diversity-oriented synthesis (DOS) library as inhibitors of scavenger receptor BI (SR-BI)-mediated lipid uptake. Bioorganic & Medicinal Chemistry Letters. 25: 2100-5
Koh MJ, Khan RK, Torker S, et al. (2015) High-value alcohols and higher-oxidation-state compounds by catalytic Z-selective cross-metathesis. Nature. 517: 181-6
Yu M, Schrock RR, Hoveyda AH. (2015) Catalyst-controlled stereoselective olefin metathesis as a principal strategy in multistep synthesis design: a concise route to (+)-neopeltolide. Angewandte Chemie (International Ed. in English). 54: 215-20
Wang C, Yu M, Kyle AF, et al. (2013) Efficient and selective formation of macrocyclic disubstituted Z alkenes by ring-closing metathesis (RCM) reactions catalyzed by Mo- or W-based monoaryloxide pyrrolide (MAP) complexes: applications to total syntheses of epilachnene, yuzu lactone, ambrettolide, epothilone C, and nakadomarin A. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2726-40
Yu M, Ibrahem I, Hasegawa M, et al. (2012) Enol ethers as substrates for efficient Z- and enantioselective ring-opening/cross-metathesis reactions promoted by stereogenic-at-Mo complexes: utility in chemical synthesis and mechanistic attributes. Journal of the American Chemical Society. 134: 2788-99
Yu M, Wang C, Kyle AF, et al. (2011) Synthesis of macrocyclic natural products by catalyst-controlled stereoselective ring-closing metathesis. Nature. 479: 88-93
Ibrahem I, Yu M, Schrock RR, et al. (2009) Highly Z- and enantioselective ring-opening/cross-metathesis reactions catalyzed by stereogenic-at-Mo adamantylimido complexes. Journal of the American Chemical Society. 131: 3844-5
See more...