Nucleophilic ring-opening of epoxides: trends in β-substituted alcohols synthesis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-09

AUTHORS

Mehdi Fallah-Mehrjardi, Ali Reza Kiasat, Khodabakhsh Niknam

ABSTRACT

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. More... »

PAGES

2033-2081

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13738-018-1400-5

DOI

http://dx.doi.org/10.1007/s13738-018-1400-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1104265842


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