Synthesis of 7-norbornenols via Diels–Alder cycloadditions of cyclopentadienol generated by decomposition of ferrocenium cation-Reference-Cited by-同舟云学术

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Synthesis of 7-norbornenols via Diels–Alder cycloadditions of cyclopentadienol generated by decomposition of ferrocenium cation

Published:2015-10 Issue:44 Volume:56 Page:6038-6042
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Allen Stacey K.,Lathrop Thomas E.,Patel Sweta B.,Harrell Moody Deanna M.,Sommer Roger D.,Coombs Thomas C.

Funder

National Science Foundation Division of Chemistry

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference65 articles.

1. 5-Fluorocyclopentadiene: synthesis and utility

2. Relative reactivities of the 5-halocyclopentadienes in diels-alder and 1,5 shift reactions

3. Antiaromaticity in the parent cyclopentadienyl cation. Reaction of 5-iodocyclopentadiene with silver ion

4. Highly Heteroatom-dependent π-Facial Stereoselectivity in the Diels–Alder Reaction of 1,3-Cyclopentadienes Having a Heteroatom Substituent at 5-Position

5. Methoxymethylation of thallous cyclopentadienide. Simplified preparation of a key intermediate for the synthesis of prostaglandins

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1. Cobalt-Functionalized Open-[60]Fullerenes;Organometallics;2024-01-04

2. Ferrocenophanium Stability and Catalysis;Molecules;2023-03-17

3. Generation of Cyclopentadiene for Diels–Alder Reactions by Visible‐Light Irradiation of Iron Sandwich Complexes;Helvetica Chimica Acta;2022-03-23

4. Pulsed-Addition ROMP: Catalytic Syntheses of Heterotelechelic Polymers via Regioselective Chain Transfer Agents;ACS Macro Letters;2022-03-22

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