Discussion Addendum for: Asymmetric Synthesis of (M)-2-Hydroxymethyl-1-(2-Hydroxy-4,6-Dimethylphenyl)Naphthalene VIAA Configurationally Unstable Biaryl Lactone-Reference-Cited by-同舟云学术

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Discussion Addendum for: Asymmetric Synthesis of (M)-2-Hydroxymethyl-1-(2-Hydroxy-4,6-Dimethylphenyl)Naphthalene VIAA Configurationally Unstable Biaryl Lactone

Published:2011-11-30 Issue: Volume: Page:70-78
ISSN:
Container-title:Organic Syntheses
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Author:

Bringmann G.¹,Gulder T.A.M.,Gulder T.

Affiliation:

1. Universty of Würzburg; Institute of Organic Chemistry; Am Hubland Würzburg Germany D-97074

Publisher

John Wiley & Sons, Inc.

Reference30 articles.

1. ASYMMETRIC SYNTHESIS OF (M)-2-HYDROXYMETHYL-1-(2-HYDROXY-4,6-DIMETHYLPHENYL)NAPHTHALENE VIA A CONFIGURATIONALLY UNSTABLE BIARYL LACTONE

2. Stereoselective Total Synthesis of Axially Chiral Natural Products via Biaryl Lactones

3. The directed synthesis of axially chiral ligands, reagents, catalysts, and natural products through the ‘lactone methodology’

4. Atroposelective Synthesis of Axially Chiral Biaryl Compounds

5. The Lactone Concept: An Efficient Pathway to Axially Chiral Natural Products and Useful Reagents

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1. Synthesis and biological evaluation of new prodrugs of etodolac and tolfenamic acid with reduced ulcerogenic potential;European Journal of Pharmaceutical Sciences;2019-12

2. Chemical Composition, Antioxidant and Antifungal Potential of Clove (Syzygium aromaticum) Essential Oil, its Major Compound and its Derivatives;Journal of Essential Oil Bearing Plants;2019-09-03

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