Journal of Computer Chemistry, Japan
Online ISSN : 1347-3824
Print ISSN : 1347-1767
ISSN-L : 1347-1767
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珍しい塩基触媒による不斉Diels-Alder合成反応のMOシミュレーション解析
染川 賢一上田 岳彦吉留 俊史石川 岳志錦織 寿
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2020 年 19 巻 4 号 p. 175-177

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The reaction process and steric situations of novel basic and chiral catalyst Diels-Alder reactions by Kagan et al. were speculated by IRC of PM7 simulation for the three molecules reactions clearly. The addition reactions of enolic dienes (1) with dienophiles (2) by amines (3) such as (S)-(+)-prolinol / (R)-(−)-prolinol proceeded via lower energy reaction complexes (RC) and transition states (TS) of two steps. The steric shapes by IRC (Figure 2 ∼ 6) showed the clear interactions between the reaction points, and of OH with amine moieties in the 1·3, 1·3·2 and TS complexes, to give high stereoselective adducts. IRC of some reactions also guesses right the Michael reaction selectivity. The handy PM7 simulation is recommended for usual chemical growth.

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