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Molybdenum-catalyzed asymmetric allylic alkylations
KTH, Superseded Departments, Chemistry.
KTH, Superseded Departments, Chemistry.ORCID iD: 0000-0002-1743-7650
2004 (English)In: Accounts of Chemical Research, ISSN 0001-4842, E-ISSN 1520-4898, Vol. 37, no 3, p. 159-167Article in journal (Refereed) Published
Abstract [en]

The highly regio- and enantioselective molybdenum-catalyzed allylic alkylation reaction has become a powerful synthetic tool during the past few years. This Account describes the achievements gained so far in the area, with special attention directed to the different chiral ligands that have been used for inducing chirality in the products, the range of allylic substrates and nucleophiles employed, mechanistic studies, and applications of the reaction in asymmetric syntheses.

Place, publisher, year, edition, pages
2004. Vol. 37, no 3, p. 159-167
Keywords [en]
fast chemistry, c-c, substitution, ligands, complexes, acetates, stereoselectivity, cyclopropanation, coordination, example
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-23262DOI: 10.1021/ar030239vISI: 000220210100003Scopus ID: 2-s2.0-1642397473OAI: oai:DiVA.org:kth-23262DiVA, id: diva2:341960
Note
QC 20100525 QC 20111101Available from: 2010-08-10 Created: 2010-08-10 Last updated: 2017-12-12Bibliographically approved

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Moberg, Christina

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