Issue 6, 2004
From the journal:

Mendeleev Communications

Taking chiral induction into the nanometre regime: chiral teleinduction in the synthesis of poly(isocyanide)s

David B. Amabilino,*a   José-Luis Serrano,b   Teresa Sierrab  and  Jaume Vecianaa  

* Corresponding authors

a Institut de Ciència de Materials de Barcelona, Consejo Superior de Investigaciones Científicas (CSIC), Bellaterra, Barcelona, Spain, Campus of Autonomous University of Barcelona, Bellatera, Barcelona, Spain
E-mail: amabilino@icmab.es

b Instituto de Ciència de Materiales de Aragön, Consejo Superior de Investigaciones Científicas (CSIC), Universidad de Zaragoza, Zaragoza, Spain, Pedro Cerbuna, 12, Zaragoza, Spain

Abstract

Diastereoselectivity in the polymerisation of isocyanides has been observed to be operating over approximately 2 nm, which separates the reactive group from the stereogenic centre, as revealed by circular dichroism spectroscopy.

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Article information

DOI
https://doi.org/10.1070/MC2004v014n06ABEH002043
Article type
Communication
Submitted
20 Sep 2004

Mendeleev Commun., 2004,14, 256-257

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Taking chiral induction into the nanometre regime: chiral teleinduction in the synthesis of poly(isocyanide)s

D. B. Amabilino, J. Serrano, T. Sierra and J. Veciana, Mendeleev Commun., 2004, 14, 256 DOI: 10.1070/MC2004v014n06ABEH002043

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