An enamide‐based domino reaction for a highly stereoselective synthesis of tetrahydropyrans

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Angewandte Chemie. International edition 58.2019, S. 13056-13059, doi:10.1002/anie.201907565, ISSN 1521-3773

Event: Veröffentlichung

(where): Frankfurt am Main

(who): Universitätsbibliothek Johann Christian Senckenberg

(when): 2019

Creator: Kramer, Philipp
Grimmer, Jennifer
Bolte, Michael
Manolikakes, Georg

URN: urn:nbn:de:hebis:30:3-561232

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 25.03.2025, 1:48 PM CET

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Associated

Kramer, Philipp
Grimmer, Jennifer
Bolte, Michael
Manolikakes, Georg
Universitätsbibliothek Johann Christian Senckenberg

Time of origin

2019

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An Enamide-BasedDomino Reactionfor aHighlyStereoselectiveSynthesisof Tetrahydropyrans

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Oxyenamides as versatile building blocks for a highly stereoselective one-pot synthesis of the 1,3-diamino-2-ol-scaffold containing three continuous stereocenters

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2-Amino-1-methyl-1H-imidazol-4(5H)-one dimethyl sulfoxide monosolvate

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An Enamide-BasedDomino Reactionfor aHighlyStereoselectiveSynthesisof Tetrahydropyrans

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Oxyenamides as versatile building blocks for a highly stereoselective one-pot synthesis of the 1,3-diamino-2-ol-scaffold containing three continuous stereocenters

Oxyenamides as Versatile Building Blocks for a Highly Stereoselective One-Pot Synthesis of the 1,3-Diamino-2-ol-Scaffold Containing Three Continuous Stereocenters

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Synthesis and crystal structure of 2-(2-hydroxyphenyl)-1,3-bis(4-methoxybenzyl)-1,3-diazinan-5-ol

2-Amino-1-methyl-1H-imidazol-4(5H)-one dimethyl sulfoxide monosolvate

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Amiloride hydrochloride methanol disolvate

2,6-Bis(2-methyl-1,3-diazinan-2-yl)-pyridine

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An enamide‐based domino reaction for a highly stereoselective synthesis of tetrahydropyrans

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Other Objects (12)

An Enamide-BasedDomino Reactionfor aHighlyStereoselectiveSynthesisof Tetrahydropyrans

Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones

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Oxyenamides as versatile building blocks for a highly stereoselective one-pot synthesis of the 1,3-diamino-2-ol-scaffold containing three continuous stereocenters

Oxyenamides as Versatile Building Blocks for a Highly Stereoselective One-Pot Synthesis of the 1,3-Diamino-2-ol-Scaffold Containing Three Continuous Stereocenters

Synthesis and Crystal Structure of 1-(3-fluorophenyl)-3-(3,4,5-trimethoxybenzoyl)thiourea

Synthesis and crystal structure of 2-(2-hydroxyphenyl)-1,3-bis(4-methoxybenzyl)-1,3-diazinan-5-ol

2-Amino-1-methyl-1H-imidazol-4(5H)-one dimethyl sulfoxide monosolvate

2,6-Diacetylpyridine-resorcinol (1/1)

2-Hydroxy­benzyl alcohol–phenanthroline (1/1)

Amiloride hydro­chloride methanol disolvate

2,6-Bis(2-methyl-1,3-diazinan-2-yl)-pyridine

An Enamide-BasedDomino Reactionfor aHighlyStereoselectiveSynthesisof Tetrahydropyrans

Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones

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Oxyenamides as versatile building blocks for a highly stereoselective one-pot synthesis of the 1,3-diamino-2-ol-scaffold containing three continuous stereocenters

Oxyenamides as Versatile Building Blocks for a Highly Stereoselective One-Pot Synthesis of the 1,3-Diamino-2-ol-Scaffold Containing Three Continuous Stereocenters

Synthesis and Crystal Structure of 1-(3-fluorophenyl)-3-(3,4,5-trimethoxybenzoyl)thiourea

Synthesis and crystal structure of 2-(2-hydroxyphenyl)-1,3-bis(4-methoxybenzyl)-1,3-diazinan-5-ol

2-Amino-1-methyl-1H-imidazol-4(5H)-one dimethyl sulfoxide monosolvate

2,6-Diacetylpyridine-resorcinol (1/1)

2-Hydroxy­benzyl alcohol–phenanthroline (1/1)

Amiloride hydro­chloride methanol disolvate

2,6-Bis(2-methyl-1,3-diazinan-2-yl)-pyridine

An Enamide-BasedDomino Reactionfor aHighlyStereoselectiveSynthesisof Tetrahydropyrans

Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones

Kompetenzen und Kompetenzabgrenzung im Hochschulinnenbereich

Oxyenamides as versatile building blocks for a highly stereoselective one-pot synthesis of the 1,3-diamino-2-ol-scaffold containing three continuous stereocenters

Oxyenamides as Versatile Building Blocks for a Highly Stereoselective One-Pot Synthesis of the 1,3-Diamino-2-ol-Scaffold Containing Three Continuous Stereocenters

Synthesis and Crystal Structure of 1-(3-fluorophenyl)-3-(3,4,5-trimethoxybenzoyl)thiourea

Synthesis and crystal structure of 2-(2-hydroxyphenyl)-1,3-bis(4-methoxybenzyl)-1,3-diazinan-5-ol

2-Amino-1-methyl-1H-imidazol-4(5H)-one dimethyl sulfoxide monosolvate

2,6-Diacetylpyridine-resorcinol (1/1)

2-Hydroxy­benzyl alcohol–phenanthroline (1/1)

Amiloride hydro­chloride methanol disolvate

2,6-Bis(2-methyl-1,3-diazinan-2-yl)-pyridine

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