Abstract
A novel class of chiral 5,5'-di(2,4,6-trialkyl)aryl salen-metal complexes have been developed and shown to catalyze highly enantioselective Nazarov cyclization reactions, giving rise to cyclopentenoids in 90:10-98:2 er. Significantly, the catalysts also promote, for the first time, highly enantioselective Nazarov reactions of "unactivated" dienones, producing hydrindenone products having in place three contiguous chiral centers.
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CITATION STYLE
Nirubana, V., Ganesamurthy, K., Ravikesavan, R., & Chitdeshwari, T. (2017). Genetic Diversity Studies in Kodo Millet (Paspalum scrobiculatum L.) Germplasm Accessions Based on Biometrical and Nutritional Quality Traits. International Journal of Current Microbiology and Applied Sciences, 6(10), 832–839. https://doi.org/10.20546/ijcmas.2017.610.099
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