Asymmetric Dearomatizing Spirolactonization of Naphthols Catalyzed by Spirobiindane-Based Chiral Hypervalent Iodine Species-Reference-Cited by-同舟云学术

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Asymmetric Dearomatizing Spirolactonization of Naphthols Catalyzed by Spirobiindane-Based Chiral Hypervalent Iodine Species

Published:2013-03-07 Issue:11 Volume:135 Page:4558-4566
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Dohi Toshifumi¹,Takenaga Naoko²,Nakae Tomofumi¹,Toyoda Yosuke¹,Yamasaki Mikio³,Shiro Motoo³,Fujioka Hiromichi²,Maruyama Akinobu²,Kita Yasuyuki¹

Affiliation:

1. College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Nojihigashi, Kusatsu, Shiga 525-8577, Japan

2. Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-oka, Suita, Osaka, Japan

3. Rigaku Corporation, 3-9-12 Matsubara, Akishima, Tokyo, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja401074u

Reference95 articles.

1. Chemistry of Polyvalent Iodine

2. Diaryliodonium Salts: A Journey from Obscurity to Fame

3. Organoiodine(V) Reagents in Organic Synthesis

4. 2-Iodoxybenzoic Acid-A Simple Oxidant with a Dazzling Array of Potential Applications

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5. Dearomatization of 3-Aminophenols for Synthesis of Spiro[chromane-3,1′-cyclohexane]-2′,4′-dien-6′-ones via Hydride Transfer Strategy-Enabled [5+1] Annulations;Molecules;2024-02-26

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