Search Results - "Funakoshi, Yuuta"
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Facile Synthesis of 2,5-Disubstituted Thiazoles from Terminal Alkynes, Sulfonyl Azides, and Thionoesters
Published in Organic letters (15-05-2015)“…A sequential procedure for the synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters is reported. A…”
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2
Synthesis of Enaminones by Rhodium-Catalyzed Denitrogenative Rearrangement of 1‑(N‑Sulfonyl-1,2,3-triazol-4-yl)alkanols
Published in Journal of the American Chemical Society (24-10-2012)“…Enaminones are synthesized by the rhodium(II)-catalyzed denitrogenative rearrangement reaction of 1-(N-sulfonyl-1,2,3-triazol-4-yl)alkanols, which are readily…”
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3
Synthesis of Elongated Esters from Alkenes
Published in Angewandte Chemie International Edition (19-11-2018)“…A convenient method for synthesizing elongated aliphatic esters from alkenes is reported. An (alkoxycarbonyl)methyl radical species is generated upon…”
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4
Thermal Reaction of 4-(p-Aminophenyl)-1-sulfonyl-1,2,3-triazoles Furnishing Benzoyl Cyanides through N-Sulfinyl Imine Intermediates
Published in Chemistry letters (05-07-2015)“…A thermal reaction of 4-(p-aminophenyl)-1-sulfonyl-1,2,3-triazoles forming benzoyl cyanides is reported. A carbene species thermally generated from the…”
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5
Site-Selective Introduction of an Enamido Group at the C(3)-Position of Indoles
Published in Heterocycles (2015)Get full text
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6
Intramolecular Dearomatizing [3 + 2] Annulation of α‑Imino Carbenoids with Aryl Rings Furnishing 3,4-Fused Indole Skeletons
Published in Journal of the American Chemical Society (12-02-2014)“…The rhodium-catalyzed dearomatizing [3 + 2] annulation reaction of 4-(3-arylpropyl)-1,2,3-triazoles is described. It provides a straightforward synthetic…”
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7
Synthesis of Penta-2,4-dien-1-imines and 1,2-Dihydropyridines by Rhodium-Catalyzed Reaction of N‑Sulfonyl-1,2,3-triazoles with 2‑(Siloxy)furans
Published in Organic letters (16-12-2016)“…A rhodium(II)-catalyzed reaction of N-sulfonyl-1,2,3-triazoles with 2-(siloxy)furans is reported. Either open-chain penta-2,4-dien-1-imines or cyclic…”
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8
Direct Production of Enaminones from Terminal Alkynes via Rhodium-Catalyzed Reaction of Formamides with N‑Sulfonyl-1,2,3-triazoles
Published in Organic letters (16-05-2014)“…A rhodium-catalyzed reaction of formamides with N-sulfonyl-1,2,3-triazoles is developed to formulate a new one-pot procedure for the direct synthesis of…”
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9
A Reaction of Triazoles with Thioesters to Produce β-Sulfanyl Enamides by Insertion of an Enamine Moiety into the Sulfur-Carbonyl Bond
Published in Angewandte Chemie International Edition (17-08-2015)“…N‐Sulfonyl‐1,2,3‐triazoles react with thioesters in the presence of a rhodium(II) catalyst to produce β‐sulfanyl enamides in a stereoselective manner. The…”
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10
A Reaction of Triazoles with Thioesters to Produce [beta]-Sulfanyl Enamides by Insertion of an Enamine Moiety into the Sulfur-Carbonyl Bond
Published in Angewandte Chemie International Edition (17-08-2015)“…N-Sulfonyl-1,2,3-triazoles react with thioesters in the presence of a rhodium(II) catalyst to produce [beta]-sulfanyl enamides in a stereoselective manner. The…”
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11
Synthesis of Elongated Esters from Alkenes
Published in Angewandte Chemie (19-11-2018)“…A convenient method for synthesizing elongated aliphatic esters from alkenes is reported. An (alkoxycarbonyl)methyl radical species is generated upon…”
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Journal Article -
12
A Reaction of Triazoles with Thioesters to Produce β-Sulfanyl Enamides by Insertion of an Enamine Moiety into the Sulfur-Carbonyl Bond
Published in Angewandte Chemie (17-08-2015)“…N‐Sulfonyl‐1,2,3‐triazoles react with thioesters in the presence of a rhodium(II) catalyst to produce β‐sulfanyl enamides in a stereoselective manner. The…”
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13
A Reaction of Triazoles with Thioesters to Produce [beta]-Sulfanyl Enamides by Insertion of an Enamine Moiety into the Sulfur-Carbonyl Bond
Published in Angewandte Chemie (17-08-2015)“…N-Sulfonyl-1,2,3-triazoles react with thioesters in the presence of a rhodium(II) catalyst to produce [beta]-sulfanyl enamides in a stereoselective manner. The…”
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