Local softness as a regioselectivity indicator in [4+2] cycloaddition reactions

被引:184
作者
Damoun, S
VandeWoude, G
Mendez, F
Geerlings, P
机构
[1] FREE UNIV BRUSSELS, FAC WETENSCHAPPEN, EENHEID ALGEMENE CHEM, B-1050 BRUSSELS, BELGIUM
[2] UNIV AUTONOMA METROPOLITANA IZTAPALAPA, DEPT QUIM, DIV CIENCIAS BASICAS & INGN, MEXICO CITY 09340, DF, MEXICO
关键词
D O I
10.1021/jp9611840
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
As part of our continuing interest in the connection between chemical reactivity and the HSAB principle, both globally and locally, we explored via 3-21 G calculations on local and global softness the statement made by Gazquez and Mendez, Their statement, claiming that two chemical species should react through atoms showing equal softness, has been precised to rationalize the regioselectivity of Normal Electron Demand Diels-Alder reactions between terminally monosubstituted 1,3-butadienes and monosubstituted ethenes. In the presence of this substitution pattern, a head-to-head mode of cyclization is largely experimentally observed, also known as ''ortho rule''. The closest values of the condensed local softness were found for the unsubstituted termini, thereby suggesting that these cycloadditions would proceed through an asynchronous pathway, as supported by transition state geometries reported by Houk et al.
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页码:886 / 893
页数:8
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