From Acyclic Precursors to Linear Triquinanes through a Diastereoselective One-Pot Process. A New Illustration of the Synthetic Power of Radical Cascades-Reference-Cited by-同舟云学术

From Acyclic Precursors to Linear Triquinanes through a Diastereoselective One-Pot Process. A New Illustration of the Synthetic Power of Radical Cascades

Published:1998-09-11 Issue:20 Volume:63 Page:6764-6765
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Devin Priscille¹,Fensterbank Louis¹,Malacria Max¹

Affiliation:

1. Laboratoire de Chimie Organique de Synthèse associé au CNRS, Université Pierre et Marie Curie, 4 place Jussieu - Tour 44-54, Case 229, 75252 Paris Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9809783

Reference26 articles.

1. Radical reactions in natural product synthesis

2. Regio- and stereo-selectivity of alkenyl radical ring closure: A theoretical study

3. Sequential free radical synthesis of a linear triquinane skeleton from an acyclic synthon

4. Tandem Radical Cyclizations: a One-Step Synthesis of Stereoisomeric Tricyclo[6.3.0.02,6]undecanes From Acyclic Precursors

Cited by 66 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 2.7 Radical Cascade Reactions;Free Radicals: Fundamentals and Applications in Organic Synthesis 2;2021

2. Radical reactions: Stereochemistry and asymmetric synthesis;Stereochemistry and Organic Reactions;2021

3. C–H functionalization reactions enabled by hydrogen atom transfer to carbon-centered radicals;Chemical Science;2020

4. The Invention of New Methodologies: An Opportunity for Dating Natural Products;Synlett;2018-08-14

5. Radical-induced expeditious stereoselective synthesis of 2-alkyl 3-allyl trans-2,3-dihydrobenzofurans (TADHBs);Synthetic Communications;2018-01-24