Efficient Coupling reactions of β-Amino and β-Acetamido Radicals with Electron Deficient Alkenes - Aza-Carbofunctionalization of Olefins - A Promising New Tool for Alkaloid Synthesis.-Reference-Cited by-同舟云学术

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Efficient Coupling reactions of β-Amino and β-Acetamido Radicals with Electron Deficient Alkenes - Aza-Carbofunctionalization of Olefins - A Promising New Tool for Alkaloid Synthesis.

Published:1983-01 Issue:20 Volume:24 Page:2051-2054
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kozikowski Alan P.,Scripko James

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Synthesis of 1,6-heterosubstituted products via radicals

2. Polare Substituenteneffekte bei der Addition von Alkyl‐Radikalen an Alkene

3. Hydroxymercuration-reductive coupling route to .delta.-lactones. Synthesis of malyngolide, an antibiotic from a marine blue-green alga

4. Irigermanal and iridogermanal: two new triterpenoids from rhizomes of Iris germanica L

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1. Synthesis of (+)-Ipalbidine Based on 6-exo-trig Radical Cyclization of a β-Amino Radical;The Journal of Organic Chemistry;2015-10-07

2. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22

3. Mercury(II) Nitrate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

4. Electrophilic cyclization of unsaturated amides;Tetrahedron;1998-11

5. Mercury;Comprehensive Organometallic Chemistry II;1995

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