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

Autoren

  • 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
Weitere Informationen

Publikationsverlauf

Received: 13. Mai 2013

Accepted after revision: 26. Juni 2013

Publikationsdatum:
26. Juli 2013 (online)


Graphical Abstract

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