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Cited by 1,050

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Organolanthanide-Catalyzed Hydroamination

Hong, Sukwon, Marks, Tobin J.·2004·Accounts of Chemical Research

Abstract

Organolanthanides are highly efficient catalysts for inter- and intramolecular hydroamination of various C-C unsaturations such as alkenes, alkynes, allenes, and dienes. Attractive features of organolanthanide catalysts include very high turnover frequencies and excellent stereoselectivities, rendering this methodology applicable to concise synthesis of naturally occurring alkaloids and other polycyclic azacycles. The general hydroamination mechanism involves turnover-limiting C-C multiple bond insertion into the Ln-N bond, followed by rapid protonolysis by other amine substrates. Sterically less encumbered ligand designs have been developed to improve reaction rates, and metallocene and nonmetallocene chiral lanthanide complexes have been synthesized for enantioselective hydroamination.

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Metadata

Authors
Hong, S., & Marks, T. J.
Venue
Accounts of Chemical Research
Published
2004-06-29
Volume
37
Issue
9
Pages
673-686
ISSN
  • 0001-4842 (ISSN-L)
  • 1520-4898
OpenAlex
W2164076542
Cited by
1,050
References
11
FWCI
39.61
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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