Diastereoselective and catalytic α-alkylation of chiral N-acyl thiazolidinethiones with stable carbocationic salts

Publication date

2019-03-04T15:22:32Z

2019-03-04T15:22:32Z

2017-06-15

2019-03-04T15:22:32Z

Abstract

Direct nickel-catalyzed alkylation of chiral N-acyl-4-isopropyl-1,3-thiazolidine-2-thiones using a commercially available nickel(II) complex, (Me3P)2NiCl2, has been developed for tropylium and trityl tetrafluoroborate salts. The reaction provides a single diastereomer of the corresponding adducts in good to high yields, which, in turn, can be easily converted into a wide array of enantiomerically pure compounds that are difficult to obtain by other asymmetric procedures.

Document Type

Article


Accepted version

Language

English

Subjects and keywords

Catàlisi; Níquel; Quiralitat; Catalysis; Nickel; Chirality

Publisher

American Chemical Society

Related items

Versió postprint del document publicat a: https://doi.org/10.1021/acs.joc.7b00657

Journal of Organic Chemistry, 2017, vol. 82, num. 12, p. 6426-6433

https://doi.org/10.1021/acs.joc.7b00657

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Rights

(c) American Chemical Society , 2017

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