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Lithium ortho ‐Lithiobenzyl Alkoxides
Author(s) -
Meyer Norbert,
Seebach Dieter
Publication year - 1978
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.197805211
Subject(s) - reagent , benzaldehyde , lithium (medication) , chemistry , phthalic acid , transformation (genetics) , organic chemistry , oxide , benzyl alcohol , combinatorial chemistry , catalysis , medicine , biochemistry , gene , endocrinology
A new lithium reagent , lithium o ‐lithiobenzyl oxide (1) , provides a facile entry to compounds of types (2) and (3). After transformation into an analogous reagent substituted benzyl alcohols react with benzaldehyde to give compounds of type (4). Products (2) to (4) cannot be synthesized from phthalic acid derivatives.
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