The stereochemistry of the addition of titanium enolates of N-propionyl-oxazolidin-2-ones to 5- and 6-membered N-acyliminium ions-Reference-Cited by-同舟云学术

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The stereochemistry of the addition of titanium enolates of N-propionyl-oxazolidin-2-ones to 5- and 6-membered N-acyliminium ions

Published:1999-04 Issue:15 Volume:40 Page:2891-2894
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Pilli Ronaldo A.,de Fátima Alves Conceição,Böckelmann Maria Alice,Mascarenhas Yvonne P.,Geraldo Nery J.,Vencato Ivo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Recent stereoselective synthetic approaches to β-amino acids

2. Recent Advances in the .beta.-Lactam Synthon Method

3. Asymmetric synthesis of building-blocks for peptides and peptidomimetics by means of the β-lactam synthon method

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1. Titanium Enolate Chemistry at the Beginning of the 21st Century;European Journal of Organic Chemistry;2016-02-24

2. Alkylation and Related Reactions II;Key Chiral Auxiliary Applications;2014

3. Diastereoselective Synthesis of β-Heteroaryl syn-α-Methyl-β-Amino Acid Derivatives via a Double Chiral Auxiliary Approach;Organic Letters;2013-01-23

4. N-tert-Butanesulfinyl Imines in Alkaloid Synthesis: Stereoselective Synthesis of (R)-Coniine and Formal Synthesis of (S)-δ-Coniceine¹;Synthesis;2011-07-14

5. A New and Efficient Synthesis of Derivatives of Octahydro-4H-pyrrolo[1,2-c]pyrido[1′,2′-a]imidazole;European Journal of Organic Chemistry;2011-03-15

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