Synthesis 2013; 45(18): 2583-2592
DOI: 10.1055/s-0033-1338507
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Functionalized Indanes via Palladium-Catalyzed Carboannulation of Diazabicyclic Olefins with o-Iodostyrenes

Eliyan Jijy
a   Organic Chemistry Section of Chemical Sciences and Technology Division, National Institute for Interdisciplinary Science and Technology (CSIR), Trivandrum 695019, India
,
Praveen Prakash
a   Organic Chemistry Section of Chemical Sciences and Technology Division, National Institute for Interdisciplinary Science and Technology (CSIR), Trivandrum 695019, India
,
Shreyass Saranya
a   Organic Chemistry Section of Chemical Sciences and Technology Division, National Institute for Interdisciplinary Science and Technology (CSIR), Trivandrum 695019, India
,
Eringathodi Suresh
b   Analytical Sciences Discipline, Central Salt and Marine Chemicals Research Institute, Bhavnagar, Gujarat 364002, India   Fax: +91(471)2491712   Email: radhu2005@gmail.com
,
Kokkuvayil Vasu Radhakrishnan*
a   Organic Chemistry Section of Chemical Sciences and Technology Division, National Institute for Interdisciplinary Science and Technology (CSIR), Trivandrum 695019, India
› Author Affiliations
Further Information

Publication History

Received: 13 May 2013

Accepted after revision: 26 June 2013

Publication Date:
26 July 2013 (online)


Abstract

Palladium-catalyzed carboannulation of bicyclic and tricyclic hydrazines with substituted o-iodostyrenes produced functionalized indanes in good to excellent yields. The methodology provides an important carbocyclic ring system under relatively mild conditions.

Supporting Information

 
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