4.4 Article

TiCl4-activated selective nucleophilic substitutions of tert-butyl alcohol and benzyl alcohols with π-donating substituents

Journal

TETRAHEDRON
Volume 66, Issue 34, Pages 6869-6872

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.06.046

Keywords

Ti(IV); Lewis acid; Alcohol

Funding

  1. National Science Council of Taiwan [NSC 98-2113-M-006-001-MY3]

Ask authors/readers for more resources

TiCl4-activated selective nucleophilic substitution reactions of tert-butyl alcohol and benzyl alcohols with pi-donating substituents in the presence of primary and secondary alcohols can be carried out with various oxygen, nitrogen and carbon nucleophiles in good yields. (C) 2010 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available