Comparative Evaluation of Pyrrole Fused Donor Moieties: 1H-Indole and Pyrrolo[2,3-<i>b</i>] Pyridine in Benzothiadiazole-Based D-A-D Type Conjugated Small Molecules for Organic Field-Effect Transistors. [PDF]
Udamulle Gedara CM +8 more
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Shape-Conserving Atom Replacements. [PDF]
Puriņš M, Elgindy C, Levin MD.
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A comprehensive review on the silane-acid reduction of alkenes in organic synthesis. [PDF]
Shingate BB.
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Research on transition metals for the multicomponent synthesis of benzo-fused γ-lactams. [PDF]
Sead FF +8 more
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Multicomponent reactions (MCRs) yielding medicinally relevant rings: a recent update and chemical space analysis of the scaffolds. [PDF]
Tandi M, Sharma V, Gopal B, Sundriyal S.
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Nonpyrogenic "Black" Nitrogen Likely Plays a Major Yet Underrecognized Role in the Global Nitrogen Cycle. [PDF]
Dos Santos JV +6 more
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Visible-light-driven NHC and organophotoredox dual catalysis for the synthesis of carbonyl compounds. [PDF]
Dhayalan V.
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Conversion of Cyclic Ketones to 2,3-Fused Pyrroles and Substituted Indoles
Journal of the American Chemical Society, 2013A highly effective synthesis of 2,3-fused pyrroles from cyclic ketones has been achieved. The transformation includes a rhodium-catalyzed reaction of 4-alkenyl-1-sulfonyl-1,2,3-triazoles featuring an unusual 4π electrocyclization. The methodology was further extended to the synthesis of indoles using a one-pot reaction starting from 1 ...
Huw M L Davies
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Bicyclization of Isocyanides: A Synthetic Strategy for Fused Pyrroles
Advanced Synthesis and Catalysis, 2011AbstractOn the isocyanide carbon atom, two CC sigma bonds are formed in the bicyclization reaction of the readily available acyclic substrates with tosylmethyl isocyanides. The reaction can proceed under extremely mild and metal‐free conditions to give the products in high to excellent yields. The powerful potential of this strategy deserves attention
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