Issue 33, 2006
From the journal:

Chemical Communications

Iodine assisted modified Suzuki type reaction of bicyclic hydrazines: stereoselective synthesis of functionalized cyclopentenes†

Jubi John,a   V. S. Sajisha,a   Smitha Mohanlala  and  K. V. Radhakrishnan*a  

* Corresponding authors

a Organic Chemistry Section, Chemical Sciences and Technology Division, Regional Research Laboratory (CSIR), Trivandrum, Kerala, India
E-mail: radhupreethi@rediffmail.com
Fax: 91-471-2491712
Tel: 91-471-2515 275

Abstract

Bicyclic hydrazines undergo a facile palladium/iodine mediated stereoselective ring opening on reaction with organoboronic acids affording trans-3,4-disubstituted hydrazino cyclopentenes in good to excellent yield.

Graphical abstract: Iodine assisted modified Suzuki type reaction of bicyclic hydrazines: stereoselective synthesis of functionalized cyclopentenes

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Article information

DOI
https://doi.org/10.1039/B607389A
Article type
Communication
Submitted
24 May 2006
Accepted
27 Jun 2006
First published
21 Jul 2006

Chem. Commun., 2006, 3510-3512

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Iodine assisted modified Suzuki type reaction of bicyclic hydrazines: stereoselective synthesis of functionalized cyclopentenes

J. John, V. S. Sajisha, S. Mohanlal and K. V. Radhakrishnan, Chem. Commun., 2006, 3510 DOI: 10.1039/B607389A

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