Exploiting Coordination Effects for the Regioselective Zincation of Diazines Using TMPZnX⋅LiX (X=Cl, Br)

Kremsmair, Alexander; Sunagatullina, Alisa S.; Bole, Leonie J; Mastropierro, Pasquale; Graßl, Simon; Wilke, Henrik R.; Godineau, Edouard; Hevia, Eva; Knochel, Paul (2022). Exploiting Coordination Effects for the Regioselective Zincation of Diazines Using TMPZnX⋅LiX (X=Cl, Br). Angewandte Chemie International Edition, 61(40), e202210491. GDCh 10.1002/anie.202210491

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A new method for regioselective zincations of challenging N-heterocyclic substrates such as pyrimidines and pyridazine was reported using bimetallic bases TMPZnX⋅LiX (TMP=2,2,6,6-tetramethylpiperidyl; X=Cl, Br). Reactions occurred under mild conditions (25-70 °C, using 1.75 equivalents of base without additives), furnishing 2-zincated pyrimidines and 3-zincated pyridazine, which were then trapped with a variety of electrophiles. Contrasting with other s-block metalating systems, which lack selectivity in their reactions even when operating at low temperatures, these mixed Li/Zn bases enabled unprecedented regioselectivities that cannot be replicated by either LiTMP nor Zn(TMP)2 on their own. Spectroscopic and structural interrogations of organometallic intermediates involved in these reactions have shed light on the complex constitution of reaction mixtures and the origins of their special reactivities.

Item Type:

Journal Article (Original Article)

Division/Institute:

08 Faculty of Science > Department of Chemistry, Biochemistry and Pharmaceutical Sciences (DCBP)

UniBE Contributor:

Bole, Leonie Julia, Mastropierro, Pasquale, Hevia Freire, Eva

Subjects:

500 Science > 570 Life sciences; biology
500 Science > 540 Chemistry

ISSN:

1433-7851

Publisher:

GDCh

Language:

English

Submitter:

Franziska Bornhauser-Rufer

Date Deposited:

08 Feb 2023 11:21

Last Modified:

12 Feb 2023 02:26

Publisher DOI:

10.1002/anie.202210491

PubMed ID:

35943036

BORIS DOI:

10.48350/178522

URI:

https://boris.unibe.ch/id/eprint/178522

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