five

Predicting the Diastereoselectivity of Rh-Mediated Intramolecular C−H Insertion

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Predicting_the_Diastereoselectivity_of_Rh-Mediated_Intramolecular_C_H_Insertion/3656307
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Rhodium-mediated cyclization of the α-diazo ester 1 proceeds with high diastereoselectivity, to give the trisubstituted cyclopentane 5. A computational model (ZINDO and Molecular Mechanics) based on our current mechanistic understanding of the reaction is presented. This model correctly predicts the dominant diastereomer from the cyclization of 1 and the eight (Table ) other α-diazo esters studied thus far.
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2016-08-18
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