Generation of the Camptothecin Scaffold by a Flavin‐Catalyzed Photooxidative Skeletal Reorganization
The biosynthetic pathway of the anticancer drug precursor camptothecin involves an enigmatic skeletal reorganization from a 6/5/6 tetrahydro‐β‐carboline to a 6/6/5 pyrroloquinoline ring system. Here, we show that this transformation can be achieved by photooxidation with flavin cofactors, such as flavin mononucleotide (FMN) as catalysts.
Shenyu Liu +6 more
wiley +1 more source
Retraction of "Effective Disposal of Methylene Blue and Bactericidal Benefits of Using GO-Doped MnO<sub>2</sub> Nanorods Synthesized through One-Pot Synthesis". [PDF]
Shaheen S +9 more
europepmc +1 more source
One-pot synthesis of sequence-controlled macromonomers <i>via</i> living anionic addition reaction and subsequent acyclic diene metathesis polymerization. [PDF]
Nishijima T +5 more
europepmc +1 more source
Versatile One-Pot Synthesis of Hydrophobic Tags by Multicomponent Reactions. [PDF]
Balestrero FC +7 more
europepmc +1 more source
One Pot Synthesis of the C-3 Complex (Curcumin, Demethoxycurcumin, and Bis-Demethoxycurcumin): Their Joint and Independent Biological Actions. [PDF]
Obregón-Mendoza MA +8 more
europepmc +1 more source
One-pot synthesis of primary phosphines from white phosphorus.
Mende M, Cammarata J, Scott DJ, Wolf R.
europepmc +1 more source
One-Pot Synthesis of Silicone-Urethane Hybrid Foam and Comparison of Flame Retardant, Rheological, and Mechanical Properties with Polyurethane Foam. [PDF]
Hwang S +7 more
europepmc +1 more source
Green One-Pot Synthesis of Benzimidazoles from Dinitroarenes in Water Using a Ru-Doped Co-Based Heterogeneous Catalyst. [PDF]
Del Río-Rodríguez JL +6 more
europepmc +1 more source
Related searches:
One Pot Synthesis of Methyl Aminoacetylcyanoacetates
Synthetic Communications, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Stylianos Hamilakis, Athanase Tsolomitis
openaire +1 more source
One-Pot Synthesis of Glucosamine Oligosaccharides
Organic Letters, 2001[reaction: see text] Tuning the reactivity of glycosyl donors derived from 2-amino-2-deoxy glucose by selective introduction of different N-protecting (NPhth and NHTroc) and anomeric leaving groups (ethylthio and phenylthio) enabled highly efficient oligosaccharide synthesis in a one-pot manner.
Micha, Fridman +3 more
openaire +2 more sources

