Asymmetric synthesis of chiral spirocyclanes: A new route to the optically active spiro[cyclopentane-1,1′-indan]-2,5-dione system-Reference-Cited by-同舟云学术

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Asymmetric synthesis of chiral spirocyclanes: A new route to the optically active spiro[cyclopentane-1,1′-indan]-2,5-dione system

Published:1996-03 Issue:11 Volume:37 Page:1817-1820
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kita Yasuyuki,Kitagaki Shinji,Imai Reiko,Okamoto Sachi,Mihara Sachiko,Yoshida Yutaka,Akai Shuji,Fujioka Hiromichi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Fredericamycin A a new antitumor antibiotic. I. Production, isolation and physicochemical properties.

2. Fredericamycin A, an antitumor antibiotic of a novel skeletal type

3. Structure of fredericamycin A, an antitumor antibiotic of a novel skeletal type. Spectroscopic and mass spectral characterization.

4. Synthesis of (.+-.)-fredericamycin A

5. Synthesis of (±) Fredericamycin A

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1. Development of New Innovative Synthetic Organic Chemistry Using Lone Pairs of Oxygen Atoms;Chemical and Pharmaceutical Bulletin;2020-10-01

2. Synthesis of 3-hydroxyindanones via potassium salt of amino acid catalyzed regioselective intramolecular aldolization of ortho-diacylbenzenes;Tetrahedron Letters;2015-02

3. ChemInform Abstract: Asymmetric Synthesis of Chiral Spirocyclanes: A New Route to the Optically Active Spiro(cyclopentane-1,1′-indan)-2,5-dione System.;ChemInform;2010-08-05

4. Asymmetric Total Synthesis of Fredericamycin A: An Intramolecular Cycloaddition Pathway;Chemistry - A European Journal;2005-10-21

5. Development of Highly Stereoselective Reactions Using Lone Pairs of Oxygen Atoms;YAKUGAKU ZASSHI;2005-09-01

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