Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

1,1-Divinylallene

Date

Authors

Cergol, Katie

Newton, Christopher

Lawrence, Andrew

Willis, Anthony

Paddon-Row, Michael

Sherburn, Michael

Publisher

Wiley-VCH Verlag GMBH

Abstract

How to hit a triple: The title hydrocarbon, one of the most π-bond-rich small molecules, has been synthesized and characterized for the first time. This highly reactive hydrocarbon undergoes a new diene-transmissive, triple Diels-Alder cycloaddition sequ

Keywords

Keywords: 1,1-divinylallene; C-C bonds; Diels-Alder cycloadditions; Diels-Alder reactions; One step; Ring systems; Small molecules; Olefins; Organic compounds; Synthesis (chemical); Cycloaddition 1,1-divinylallene; cycloaddition; Diels-Alder reactions; hydrocarbons

URI

http://hdl.handle.net/1885/60369

Collections

ANU Research Publications

Source

Angewandte Chemie International Edition

Type

Journal article

DOI

10.1002/anie.201105541

Restricted until

2037-12-31

Downloads

File

Description

01_Cergol_1,1-Divinylallene_2011.pdf (581.23 KB)