Arylglyoxals in synthesis of heterocyclic compounds
Heterocycles are an extraordinarily important class of compounds, making up more than half
of all known organic compounds. Heterocycles are present in a wide variety of drugs, most …
of all known organic compounds. Heterocycles are present in a wide variety of drugs, most …
Asymmetric carbon–carbon bond formation under continuous‐flow conditions with chiral heterogeneous catalysts
T Tsubogo, T Ishiwata… - Angewandte Chemie …, 2013 - Wiley Online Library
Catalytic asymmetric carbon–carbon bond‐forming reactions provide one of the most
efficient ways to synthesize optically active compounds, and, accordingly, many chiral …
efficient ways to synthesize optically active compounds, and, accordingly, many chiral …
Chiral paddle-wheel diruthenium complexes for asymmetric catalysis
T Miyazawa, T Suzuki, Y Kumagai, K Takizawa… - Nature Catalysis, 2020 - nature.com
The development of robust and reactive chiral catalysts is a fundamental aim in asymmetric
catalysis, and crucial for providing efficient methods for synthesizing chiral molecules. Chiral …
catalysis, and crucial for providing efficient methods for synthesizing chiral molecules. Chiral …
Dirhodium: carbene transformations and beyond
R Wu, D Zhu, S Zhu - Organic Chemistry Frontiers, 2023 - pubs.rsc.org
Dirhodiums, which feature lantern-or paddlewheel-like structures, have emerged as a class
of useful catalysts in organic synthesis. Among the transformations catalyzed by dirhodiums …
of useful catalysts in organic synthesis. Among the transformations catalyzed by dirhodiums …
High symmetry dirhodium (II) paddlewheel complexes as chiral catalysts
The design and use of chiral dirhodium (II) paddlewheel complexes as catalysts for
asymmetric metal carbenoid and metal nitrenoid reactions, and as Lewis acids have …
asymmetric metal carbenoid and metal nitrenoid reactions, and as Lewis acids have …
Perspective on dirhodium carboxamidates as catalysts
MP Doyle - The Journal of organic chemistry, 2006 - ACS Publications
Dirhodium compounds are emerging as highly efficient catalysts for diverse reactions, and
those with carboxamidate ligands have the broadest applications. The unique features of …
those with carboxamidate ligands have the broadest applications. The unique features of …
Forty years after “Heterodiene syntheses with α, β-unsaturated carbonyl compounds”: enantioselective syntheses of 3, 4-dihydropyran derivatives
G Desimoni, G Faita, P Quadrelli - Chemical reviews, 2018 - ACS Publications
This review is focused on the enantioselective synthesis of 3, 4-dihydropyran derivatives,
whose importance as chiral building blocks in the synthesis of bioactive molecules and …
whose importance as chiral building blocks in the synthesis of bioactive molecules and …
Asymmetric hetero-Diels–Alder reactions of carbonyl compounds
H Pellissier - Tetrahedron, 2009 - Elsevier
Since its discovery in 1928 by Diels and Alder, 1 the Diels–Alder reaction has become one
of the cornerstone reactions in organic chemistry for the construction of six-membered rings …
of the cornerstone reactions in organic chemistry for the construction of six-membered rings …
Dirhodium (II) tetrakis [N-tetrachlorophthaloyl-(S)-tert-leucinate]: a new chiral Rh (II) catalyst for enantioselective amidation of C H bonds
M Yamawaki, H Tsutsui, S Kitagaki, M Anada… - Tetrahedron letters, 2002 - Elsevier
Dirhodium (II) tetrakis [N-tetrachlorophthaloyl-(S)-tert-leucinate], characterized by
substitution of chlorine atoms for four hydrogen atoms on the phthalimido group in the parent …
substitution of chlorine atoms for four hydrogen atoms on the phthalimido group in the parent …
Examination of the Mechanism of Rh2(II)-Catalyzed Carbazole Formation Using Intramolecular Competition Experiments
BJ Stokes, KJ Richert, TG Driver - The Journal of organic …, 2009 - ACS Publications
The use of a rhodium (II) carboxylate catalyst enables the mild and stereoselective formation
of carbazoles from biaryl azides. Intramolecular competition experiments of triaryl azides …
of carbazoles from biaryl azides. Intramolecular competition experiments of triaryl azides …