Abstract
Stereoselectivities of (4+2) cycloaddition reactions of cyclopentadiene with the methyl-substituted allenic acids and esters were investigated by application of $\pi$-nonbonded interaction ($\pi$-NBI) theory. 2-FMO method has been found to be adequate for determination of endo selectivities of diene(LUMO)-dienophile (LUMO) interaction in the thermal reactions and diene (HOMO)-dienophile (LUMO) interaction in the Lewis acid catalyzed reactions. $\pi$-isoconjugate diene structure was formed by through-bond interaction of allene moiety with methyl group in the cumulated diene system; the methyl substituent acts as a conjugative chain and causes inter-level narrowing effect of the FMO's. In dienophiles which do not form $\pi$-isoconjugate diene system, methyl group acts merely as an electron donating group. In thermal reactions, the stereoselectivities are controlled by $\pi$-nonbonded secondary orbital interaction ($\pi$-NSOI) of methyl substituent, which behaves similarly as an ethylene molecule.
시클로로펜타디엔과 메틸기로 치환된 알렌의 산 및 에스테르간의 (4+2)고리화반응에서 입체 선택성을 $\pi$-비결합상호작용($\pi$-NBI)을 적용하여 고찰하였다. 열반응에서는 diene(LUMO)-dienophile (HOMO)만을 고려한 2-FMO방법이, 산촉매반응에서는 diene (HOMO)-dienophile (LUMO)상호작용만을 고려한 2-FMO방법이 이들의 입체선택성의 결정에 중요하였다. cumulated diene계의 친디엔체에서 메틸 치환기는 알렌구조와 through-bond 상호작용에 의해 $\pi$-isoconjugate diene 구조를 형성하여 컨쥬게이션기로 작용하며 FMO의 에너지에 narrowing effect를 주고 있으나 이같은 $\pi$-isoconjugated diene 구조를 만들 수 없는 친디엔체에서는 메틸기가 단순히 전자주는기로 작용한다. 열반응에서 입체선택성은 에틸렌 분자와 마찬가지로 메틸 치환기의 $\pi$-비결합 2차궤도 상호작용($\pi$-NSOI)에 의해서 좌우되었다.