Synthesis of highly functionalized [3]dendralenes and their Diels–Alder reactions displaying unexpected regioselectivity-Reference-Cited by-同舟云学术

Synthesis of highly functionalized [3]dendralenes and their Diels–Alder reactions displaying unexpected regioselectivity

Published:2016 Issue:43 Volume:6 Page:37136-37148
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Naidu Gonna Somu¹²³⁴,Singh Rekha¹²³⁴,Kumar Mukesh⁵²³⁴,Ghosh Sunil K.¹²³⁴

Affiliation:

1. Bio-Organic Division

2. Bhabha Atomic Research Centre

3. Mumbai 400085

4. India

5. Solid State Physics Division

Abstract

Sequential olefinations were applied for the synthesis of acyclic tetrasubstituted [3]dendralenes, which did not cyclodimerize and displayed unusual regioselectivity in the Diels–Alder reaction.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA01729K

Reference64 articles.

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2. Dendralenes: The Breakthrough

3. Forgotten hydrocarbons prepared

4. Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity

5. Demystifying the dendralenes

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