Results 231 to 240 of about 14,141 (248)
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Organic and biomolecular chemistry, 2016
The synthesis of oxazolines and oxazines from N-allylamides was accomplished via an unprecedented reaction set. This reaction involved an intramolecular cyclization of N-allylamides resulting from nucleophilic attack of the allylamine on the benzoxazin-4-
J. Ranjith+3 more
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The synthesis of oxazolines and oxazines from N-allylamides was accomplished via an unprecedented reaction set. This reaction involved an intramolecular cyclization of N-allylamides resulting from nucleophilic attack of the allylamine on the benzoxazin-4-
J. Ranjith+3 more
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Journal of Organic Chemistry, 2016
This paper describes the stereoselective total syntheses of (+)-1-deoxygalactonojirimycin and (-)-1-deoxygulonojirimycin via new chiral building blocks syn,anti,syn-oxazine 11a and syn,syn,anti-oxazine 13a.
Jin-Seok Kim+7 more
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This paper describes the stereoselective total syntheses of (+)-1-deoxygalactonojirimycin and (-)-1-deoxygulonojirimycin via new chiral building blocks syn,anti,syn-oxazine 11a and syn,syn,anti-oxazine 13a.
Jin-Seok Kim+7 more
semanticscholar +1 more source
Environmental Chemistry Letters, 2021
B. Saikia, Mohit L. Deb, P. Baruah
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B. Saikia, Mohit L. Deb, P. Baruah
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, 2016
Silyl nitronates undergo rhodium-catalyzed formal [3+3]-cycloaddition with enol diazoacetates to form N-silyloxy-3,6-dihydro-2H-1,2-oxazines. The scope of the reaction and the extent of the major side process were evaluated.
Alexander S. Shved+5 more
semanticscholar +1 more source
Silyl nitronates undergo rhodium-catalyzed formal [3+3]-cycloaddition with enol diazoacetates to form N-silyloxy-3,6-dihydro-2H-1,2-oxazines. The scope of the reaction and the extent of the major side process were evaluated.
Alexander S. Shved+5 more
semanticscholar +1 more source
Chemical Communications, 2015
A Pd-catalyzed highly regioselective 6-exo-dig cyclization/alkenylation reaction of ortho-ethynylanilides has been developed. This tandem cross-coupling protocol represents a simple, efficient, step- and atom-economic approach for the construction of ...
Zhong-Jian Cai+3 more
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A Pd-catalyzed highly regioselective 6-exo-dig cyclization/alkenylation reaction of ortho-ethynylanilides has been developed. This tandem cross-coupling protocol represents a simple, efficient, step- and atom-economic approach for the construction of ...
Zhong-Jian Cai+3 more
semanticscholar +1 more source
Organic Letters, 2014
Rhodium-catalyzed transannulation of 1,2,3-triazoles and ring-opening reactions of epoxides is described. A number of 3,4-dihydro-2H-1,4-oxazines are obtained in moderate yields probably involving generation of α-imino rhodium(II) carbene species.
Xueji Ma+3 more
semanticscholar +1 more source
Rhodium-catalyzed transannulation of 1,2,3-triazoles and ring-opening reactions of epoxides is described. A number of 3,4-dihydro-2H-1,4-oxazines are obtained in moderate yields probably involving generation of α-imino rhodium(II) carbene species.
Xueji Ma+3 more
semanticscholar +1 more source
Chemical Communications, 2014
A novel method for direct C-H functionalization of saturated N-heterocycles allowing easy access to synthetically as well as biologically important and structurally diverse ring-fused oxazines is developed.
Sujit Mahato, Surajit Haldar, C. Jana
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A novel method for direct C-H functionalization of saturated N-heterocycles allowing easy access to synthetically as well as biologically important and structurally diverse ring-fused oxazines is developed.
Sujit Mahato, Surajit Haldar, C. Jana
semanticscholar +1 more source
, 2015
The novel spirooxindoline fused [1,3]oxazines were efficiently synthesized from Diels-Alder reaction of N-arylmaleimides with 1,2-dihydro-2-oxospiro[3H-indole-3,2′-[2H,9aH-pyrido[2,1-b][1,3]oxazines], which were generated in situ from three-component ...
Jing Sun, Hui Gong, Chaoguo Yan
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The novel spirooxindoline fused [1,3]oxazines were efficiently synthesized from Diels-Alder reaction of N-arylmaleimides with 1,2-dihydro-2-oxospiro[3H-indole-3,2′-[2H,9aH-pyrido[2,1-b][1,3]oxazines], which were generated in situ from three-component ...
Jing Sun, Hui Gong, Chaoguo Yan
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, 2014
3,6-Dihydro-2H-1,2-oxazines were synthesised via solid-phase synthesis to afford mixtures of stereo- and regioisomers. The analytical conditions for the analysis of the isomer ratio suitable for checking of reaction conditions of possible stereoselective
Aidan Harrison+3 more
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3,6-Dihydro-2H-1,2-oxazines were synthesised via solid-phase synthesis to afford mixtures of stereo- and regioisomers. The analytical conditions for the analysis of the isomer ratio suitable for checking of reaction conditions of possible stereoselective
Aidan Harrison+3 more
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Becher's investigations upon the soluble metallic lakes of the oxazines have been re-investigated, extended and results described. Gallamin blue, gallocyanin and coelestin blue in combination with ferric ammonium sulfate gave the best results.
F. Phoescheh, A. S. Arkush
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