Synfacts 2017; 13(04): 0377
DOI: 10.1055/s-0036-1590153
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Synergistic Iridium and Lewis Base Catalyzed Stereodivergent Allylic Substitutions

Contributor(s):
Hisashi Yamamoto
,
Hiroaki Tsuji
Jiang X. Beiger JJ. Hartwig JF. * University of California, Berkley, USA
Stereodivergent Allylic Substitutions with Aryl Acetic Acid Esters by Synergistic Iridium and Lewis Base Catalysis.

J. Am. Chem. Soc. 2017;
139: 87-90
Further Information

Publication History

Publication Date:
17 March 2017 (online)

 

Significance

Catalytic asymmetric construction of all possible stereoisomers by a simple and unified method is a challenging research subject in synthetic organic chemistry. The authors developed a stereodivergent allylic substitution with arylacetic acid esters and synergistic iridium/­benzotetramisole (BTM) catalysis.


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Comment

The reaction proceeded in the presence of ent-[Ir]-1 and (R)-BTM as synergistic catalysts to give the corresponding products bearing two adjacent stereocenters in high yields and with excellent stereoselectivities. The catalyst system permitted the synthesis of all four stereoisomers of the products. Iridium complex [Ir]-2 also showed catalytic performance in the stereodivergent allylic substitutions.


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