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Chiral trialkoxysilanols derived from terpene alcohols. Molecular structures of tris([(1S)-endo]-(-)-bornoxy)silanol and tetrakis((-)-menthoxy)silane

Version 2 2024-06-16, 13:43
Version 1 2014-10-27, 16:26
journal contribution
posted on 2024-06-16, 13:43 authored by J Beckmann, D Dakternieks, E Tiekink
Terpene alcohols (−)-menthol and [(1S)-endo]-(−)-borneol react with SiCl4 in the presence of base to give (MenO)3SiCl (1) and (BorO)3SiCl (2) in high yields. Hydrolysis of 1 yields (MenO)3SiOH (4) and (MenO)4Si (3). Hydrolysis of 2 yields only (BorO)3SiOH (5). The crystal structures of 3 and 5 are reported.


History

Alternative title

Chiral trialkoxysilanols derived from terpene alcohols. Molecular structures of tris([(1S)-endo]-(-)-bornoxy)silanol and tetrakis((-)-menthoxy)silane

Journal

Journal of organometallic chemistry

Volume

648

Pagination

188-192

Location

New York, N.Y.

ISSN

0022-328X

eISSN

1872-8561

Language

eng

Publication classification

C1 Refereed article in a scholarly journal

Copyright notice

2002, Elsevier Science B.V.

Issue

1-2

Publisher

Elsevier Science SA

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