Maximum Symmetrical Split of Molecular Graphs. Application to Organic Synthesis Design

Author:

Vismara Philippe1,Tognetti Yannic1,Laurenço Claude1

Affiliation:

1. Laboratoire d'Informatique, de Robotique et de Microélectronique de Montpellier (LIRMM), UMR 5506 CNRS/Université Montpellier II, 161 rue Ada, 34392 Montpellier Cedex 5, France, Laboratoire des Systèmes d'Information Chimique (LSIC), UMR 5076 CNRS/Ecole Nationale Supérieure de Chimie de Montpellier, 8 rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France, and Ecole Nationale Supérieure d'Agronomie de Montpellier (ENSA-M), place Pierre Viala, 34060 Montpellier Cedex 1, France

Publisher

American Chemical Society (ACS)

Subject

Library and Information Sciences,Computer Science Applications,General Chemical Engineering,General Chemistry

Reference60 articles.

1. Spatial Arrangement and Preparative Organic Synthesis

2. Systematic synthesis design. 6. Yield analysis and convergency

3. Synthons have been defined by Corey as “structural units within molecules which can be formed and/or assembled by known or conceivable synthetic operations”.9Because of its general definition, this term has been (mis)interpreted in various ways, causing some confusion. Originally, it was used by Corey in the context of retrosynthesis to refer to both structural features of a target to which the transforms may be keyed (these substructures were later renamedretrons) and structural fragments that could result from bond disconnections. In this paper, it is used according to the second meaning. This is consistent with the synthon approach to organic synthesis as described in Warren's classic book:  Warren, S.Organic Synthesis:  The Disconnection Approach; Wiley:  Chichester, U.K., 1982.

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