Stable enols from Grignard addition to 1,2-diesters: serendipity rules-Reference-Cited by-同舟云学术

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Stable enols from Grignard addition to 1,2-diesters: serendipity rules

Published:2003-08 Issue:34 Volume:59 Page:6433-6443
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Nicaise Olivier J.-C,Mans Douglas M,Morrow Andrew D,Hefti Emilio Villa,Palkovacs Elizabeth M,Singh Rajesh K,Zukowska Malgorzata A,Morin Matthew D

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference39 articles.

1. Serendipity: Accidental Discoveries in Science;Roberts,1989

2. An Amino Alcohol Ligand for Highly Enantioselective Addition of Organozinc Reagents to Aldehydes: Serendipity Rules

3. Photochemical electrocyclization of 1,4,6-trisubstituted pyrimidin-2-ones to 2-oxo-1,3-diazabicyclo[2.2.0]hex-5-enes

4. A New Method for the Synthesis of the 1,3-Diazetidin-2-ones by the Ozonolysis of the 2-Oxo-1,3-diazabicyclo[2.2.0]hex-5-enes

5. Synthesis of 1,3-diazetidin-2-ones (aza-β-lactams) as rationally designed transpeptidase and β-lactamase inhibitors

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3. Optimization of Grignard Addition to Esters: Kinetic and Mechanistic Study of Model Phthalide Using Flow Chemistry;Industrial & Engineering Chemistry Research;2018-03-21

4. Total synthesis of pipecolic acid and 1-C-alkyl 1,5-iminopentitol derivatives by way of stereoselective aldol reactions from (S)-isoserinal;Organic & Biomolecular Chemistry;2018

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