Alk‐2‐ynyl Trimethylsilyl Chalcogenoethers by Nucleophilic Substitution of Propargyl Bromides | Zendy

Taher Deeb | Zendy; Wallbank Andrew I. | Zendy; Turner Elizabeth A. | Zendy; Cuthbert Heather L. | Zendy; Corrigan John F. | Zendy

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Alk‐2‐ynyl Trimethylsilyl Chalcogenoethers by Nucleophilic Substitution of Propargyl Bromides

Author(s) -

Taher Deeb,

Wallbank Andrew I.,

Turner Elizabeth A.,

Cuthbert Heather L.,

Corrigan John F.

Publication year - 2006

Publication title -

european journal of inorganic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.667

H-Index - 136

eISSN - 1099-0682

pISSN - 1434-1948

DOI - 10.1002/ejic.200600583

Subject(s) - chemistry , propargyl , trimethylsilyl , thermal decomposition , yield (engineering) , lithium (medication) , nucleophile , nucleophilic substitution , medicinal chemistry , organic chemistry , catalysis , medicine , materials science , metallurgy , endocrinology

Lithium (trimethylsilyl)chalcogenolates have been generated and used to prepare a series of alk‐2‐ynyl trimethylsilyl chalcogenoethers from the corresponding propargyl bromides in good yield. The thermal decomposition of the telluroethers has also been studied. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)

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