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

Chen Yu Tsai; Robert Sung; Bo Ren Zhuang; Kuangsen Sung

doi:10.1016/j.tet.2010.06.046

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

Chen Yu Tsai, Robert Sung, Bo Ren Zhuang, Kuangsen Sung

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

21 Citations (Scopus)

Abstract

TiCl₄-activated selective nucleophilic substitution reactions of tert-butyl alcohol and benzyl alcohols with π-donating substituents in the presence of primary and secondary alcohols can be carried out with various oxygen, nitrogen and carbon nucleophiles in good yields.

Original language	English
Pages (from-to)	6869-6872
Number of pages	4
Journal	Tetrahedron
Volume	66
Issue number	34
DOIs	https://doi.org/10.1016/j.tet.2010.06.046
Publication status	Published - 2010 Aug 21

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tet.2010.06.046

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

abstract = "TiCl4-activated selective nucleophilic substitution reactions of tert-butyl alcohol and benzyl alcohols with π-donating substituents in the presence of primary and secondary alcohols can be carried out with various oxygen, nitrogen and carbon nucleophiles in good yields.",

author = "Tsai, {Chen Yu} and Robert Sung and Zhuang, {Bo Ren} and Kuangsen Sung",

note = "Funding Information: Financial support from National Science Council of Taiwan ( NSC 98-2113-M-006-001-MY3 ) is gratefully acknowledged. ",

year = "2010",

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T1 - TiCl4-activated selective nucleophilic substitutions of tert-butyl alcohol and benzyl alcohols with π-donating substituents

AU - Tsai, Chen Yu

AU - Sung, Robert

AU - Zhuang, Bo Ren

AU - Sung, Kuangsen

N1 - Funding Information: Financial support from National Science Council of Taiwan ( NSC 98-2113-M-006-001-MY3 ) is gratefully acknowledged.

PY - 2010/8/21

Y1 - 2010/8/21

N2 - TiCl4-activated selective nucleophilic substitution reactions of tert-butyl alcohol and benzyl alcohols with π-donating substituents in the presence of primary and secondary alcohols can be carried out with various oxygen, nitrogen and carbon nucleophiles in good yields.

AB - TiCl4-activated selective nucleophilic substitution reactions of tert-butyl alcohol and benzyl alcohols with π-donating substituents in the presence of primary and secondary alcohols can be carried out with various oxygen, nitrogen and carbon nucleophiles in good yields.

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U2 - 10.1016/j.tet.2010.06.046

DO - 10.1016/j.tet.2010.06.046

M3 - Article

AN - SCOPUS:77955468738

SN - 0040-4020

VL - 66

SP - 6869

EP - 6872

JO - Tetrahedron

JF - Tetrahedron

IS - 34

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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