A highly diastereoselective synthesis of tricyclic lactams and their application as novel N-acyl iminium ion precursors in the synthesis of isoindolinone derivatives-Reference-Cited by-同舟云学术

A highly diastereoselective synthesis of tricyclic lactams and their application as novel N-acyl iminium ion precursors in the synthesis of isoindolinone derivatives

Published:1997-05 Issue:20 Volume:38 Page:3627-3630
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Allin Steven M,Northfield Christopher J,Page Michael I,Slawin Alexandra M.Z

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. An unexpected Mitsunobu reaction. A direct route to the 2,5-diazabicyclo[2.2.1]heptan-3-one skeleton as a γ-lactam mimic of β-lactam antibiotics

2. Neighbouring Group Assistance in the Formation of Phthalimidines from o-Phthalaldehyde: an ”Intramolecular Auxiliary Effect”

3. A simple asymmetric synthesis of 2-substituted pyrrolidines from 3-acylpropionic acids

4. A simple asymmetric synthesis of 2-substituted pyrrolidines and 5-substituted pyrrolidinones

5. Asymmetric synthesis of spiro 2-pyrrolidin-5-ones and 2-piperidin-6-ones

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