Nucleophilic Addition to (3-Methylpentadienyl)iron(1+) Cations: Counterion Control of Regioselectivity; Application to the Enantioselective Synthesis of 4,5-Disubstituted Cyclohexenones-Reference-Cited by-同舟云学术

Nucleophilic Addition to (3-Methylpentadienyl)iron(1+) Cations: Counterion Control of Regioselectivity; Application to the Enantioselective Synthesis of 4,5-Disubstituted Cyclohexenones

Published:2006-04-14 Issue:18 Volume:128 Page:5984-5985
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Chaudhury Subhabrata¹,Donaldson William A.¹

Affiliation:

1. Department of Chemistry, Marquette University, P.O. Box 1881, Milwaukee, Wisconsin 53201-1881

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja055668y

Reference25 articles.

1. CC bond formation using allylic organozirconium compounds. Nucleophilic additions on to isolated and in situ generated η5-pentadienyl-Fe(CO)3/Fe(CO)2PPh3(+1) cations

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