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Stereochemistry and Reactivity of the HPA-Imine Mannich Intermediate.


ABSTRACT: Homophthalic anhydride (HPA) typically reacts rapidly with benzalimines to afford the formal [4+2] adduct, a 1,2,3,4-tetrahydroisoquinolin-1-one-4-carboxylic acid. The stereochemical outcome of this reaction is consistent with an open transition state comprising an iminium species and enolized HPA, leading to a short-lived amino-anhydride intermediate. In the case of N-tert-butylbenzalimine, this Mannich-type intermediate, which would normally cyclize at low temperature to a single isomer of the delta-lactam, is intercepted by base treatment to afford beta-lactam products. A pathway featuring ketene formation followed by ring closure is implicated.

SUBMITTER: Polyak D 

PROVIDER: S-EPMC5737782 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature

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Stereochemistry and Reactivity of the HPA-Imine Mannich Intermediate.

Polyak Daniel D   Phung Ngan N   Liu Jian J   Barrows Robert R   Emge Thomas J TJ   Knapp Spencer S  

Tetrahedron letters 20170831 40


Homophthalic anhydride (HPA) typically reacts rapidly with benzalimines to afford the formal [4+2] adduct, a 1,2,3,4-tetrahydroisoquinolin-1-one-4-carboxylic acid. The stereochemical outcome of this reaction is consistent with an open transition state comprising an iminium species and enolized HPA, leading to a short-lived amino-anhydride intermediate. In the case of <i>N</i>-<i>tert</i>-butylbenzalimine, this Mannich-type intermediate, which would normally cyclize at low temperature to a single  ...[more]

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