M
Mohammad Movassaghi
Researcher at Massachusetts Institute of Technology
Publications - 178
Citations - 7155
Mohammad Movassaghi is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Total synthesis & Enantioselective synthesis. The author has an hindex of 48, co-authored 172 publications receiving 6391 citations. Previous affiliations of Mohammad Movassaghi include Harvard University & Scripps Research Institute.
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Journal ArticleDOI
Direct synthesis of pyridine derivatives.
TL;DR: A single-step conversion of various N-vinyl and N-aryl amides to the corresponding pyridine and quinoline derivatives, respectively is described.
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Total synthesis of (+)-11,11'-dideoxyverticillin A.
TL;DR: This work reports a concise enantioselective total synthesis of (+)-11,11′-dideoxyverticillin A via a strategy inspired by the biosynthetic hypothesis for this alkaloid through a rapid functionalization of the advanced molecular framework.
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Pd(II)-catalyzed meta-C-H olefination, arylation, and acetoxylation of indolines using a U-shaped template
Guoqiang Yang,Petra Lindovska,Dajian Zhu,Justin Kim,Peng Wang,Ri-Yuan Tang,Mohammad Movassaghi,Jin-Quan Yu +7 more
TL;DR: A wide range of synthetically important and advanced indoline analogues are selectively functionalized at the meta-positions because of the combination of a monoprotected amino acid ligand and the nitrile template attached at the indolinyl nitrogen via a sulfonamide linkage.
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N-heterocyclic carbene-catalyzed amidation of unactivated esters with amino alcohols.
TL;DR: A series of solution studies in addition to the first X-ray structure of a carbene-alcohol complex support acarbene-base nucleophile activation mechanism.
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Synthesis of Substituted Pyridine Derivatives via the Ruthenium-Catalyzed Cycloisomerization of 3-Azadienynes
TL;DR: A two-step conversion of various N-vinyl and N-aryl amides to the corresponding substituted pyridines and quinolines, respectively is described, resulting in a wide range of new alkynyl imines.