A Novel and Convenient Chemoselective Deprotection Method for Both Silyl and Acetyl Groups on Acidic Hydroxyl Groups Such as Phenol and Carboxylic Acid by Using a Nitrogen Organic Base, 1,1,3,3-Tetramethylguanidine-Reference-Cited by-同舟云学术

A Novel and Convenient Chemoselective Deprotection Method for Both Silyl and Acetyl Groups on Acidic Hydroxyl Groups Such as Phenol and Carboxylic Acid by Using a Nitrogen Organic Base, 1,1,3,3-Tetramethylguanidine

Published:2003-01-01 Issue:2 Volume:5 Page:209-212
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Oyama Kin-ichi¹,Kondo Tadao¹

Affiliation:

1. Chemical Instrument Center, Nagoya University, Chikusa, Nagoya 464-8602, Japan, and Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol027263d

Reference16 articles.

1. Relative Hydride, Proton, and Hydrogen Atom Transfer Abilities of [HM(diphosphine)2]PF6 Complexes (M = Pt, Ni)

2. Protective Groups in Organic Synthesis

3. (b) Kocienski, P. J.Protecting Groups; George Thieme Verlag: New York, 1994.

4. Glycoscience

5. Selective deprotection of alcoholic and phenolic silyl ethers

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