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Nucleophilic ring-opening of epoxides: trends in -substituted alcohols synthesis
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The present review deals with the ring-opening of epoxides by various carbon, nitrogen, oxygen, halogen, and sulfur-containing nucleophiles, which most of the resulting products are versatile intermediates in the synthesis of various biologically active compounds. The regioselectivity and environmentally benign nature of procedures for the synthesis of similar products have been also discussed in detail.
Researchers Khodabakhsh Niknam (Third researcher)