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April 17, 2001Angewandte Chemie International Edition118 citations

A Novel and Highly Stereoselective Intramolecular Formal 3+3 Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin

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LWLin‐Li WeiRHRichard P. HsungHSHeather M. Sklenicka

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Abstract

Complex piperidinyl heterocycles (for example, 2) were accessed by using a novel intramolecular formal 3+3 cycloaddition reaction of vinylogous amides tethered with enals (for example, 1). This method has been applied to a formal total synthesis of (+)-gephyrotoxin (3).

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Wei et al. (2001) studied this question.

synapsesocial.com/papers/6a6e219c35aa2c282ce02741https://doi.org/10.1002/1521-3773(20010417)40:8<1516::aid-anie1516>3.0.co;2-v
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