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Updated: Jul 7, 2026

A Strategy for Sensitive, Large Scale Quantitative Metabolomics
14:18

A Strategy for Sensitive, Large Scale Quantitative Metabolomics

Published on: May 27, 2014

(-) -ミカラミドAの正式な合成である

Barry M Trost1, Hanbiao Yang, Gary D Probst

  • 1Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. bmtrost@stanford.edu

Journal of the American Chemical Society
|January 8, 2004
PubMed
まとめ

研究者らは,複雑な分子である (-) - マイカラミドA の効率的な合成戦略を開発した. 重要なステップは,コア構造の構築のために,地域選択的カップリングとディアステレオ選択的サイクライゼーションを含む.

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Carboxylic Acid Derivatives: Overview

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Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides

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The IUPAC and common names of acid halides are derived from the corresponding carboxylic acids, by changing “ic acid” to “yl halide.” For example, as shown below, the IUPAC name ethanoyl chloride is derived from ethanoic acid, and the common name, acetyl chloride, is obtained from acetic acid.
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Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles

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The IUPAC and common names of amides are derived from the parent carboxylic acid, by replacing the suffix “oic acid” and “ic acid,” respectively, with “amide.” In the following example, the IUPAC name ethanamide is derived from ethanoic acid, and the common name, acetamide, is obtained from acetic acid.
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Amino Acid Biosynthetic Pathways

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