Novel ipso-Substitution of p-Sulfinylphenols through the Pummerer-Type Reaction: A Selective and Efficient Synthesis of p-Quinones and Protected p-Dihydroquinones-Reference-Cited by-同舟云学术

Novel ipso-Substitution of p-Sulfinylphenols through the Pummerer-Type Reaction: A Selective and Efficient Synthesis of p-Quinones and Protected p-Dihydroquinones

Published:1997-08-01 Issue:16 Volume:62 Page:5526-5536
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Akai Shuji¹,Takeda Yoshifumi¹,Iio Kiyosei¹,Takahashi Kenji¹,Fukuda Nobuhisa¹,Kita Yasuyuki¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Osaka University, 1-6, Yamada-oka, Suita, Osaka 565, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo970418o

Reference46 articles.

1. Naturally Occurring Naphthazarins. Synthesis of (±)-Ventiloquinones C, D, E and G

2. Oxidations with potassium nitrosodisulfonate (Fremy's radical). Teuber reaction.

3. Efficient, regiospecific synthesis of anthracycline intermediates: total synthesis of daunomycin

4. Synthesis of azanzone A, a new naturally occurring o-naphthoquinone

5. An expeditious synthesis of javanicin

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