Amino Acids and Peptides. VII. Phosphorus in Organic Synthesis. II. A New Method for the Synthesis of Peptides using the Adducts of Phosphorus Compounds and Tetrahalomethanes

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概要

• 論文の詳細を見る

• The adducts of phosphorus compounds and tetrahalomethanes were applied to peptide synthesis as condensation reagents. Several kinds of phosphorus compounds, tetrahalomethanes, bases, and solvents were investigated for the Young racemization test and the racemization-free reaction conditions were established.

• 公益社団法人日本薬学会の論文
• 1974-04-25

著者

• 山田 俊一

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 山田 俊一

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 竹内 義雄

  Faculty Of Pharmaceutical Sciences University Of Tokyo

関連論文

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• Studies on Optically Active Amino Acids. V. Synthesis of Optically Active α-Aminoalcohols by the Reduction of α-Amino Acid Esters with Sodium Borohydride
• Studies on Optically Active Amino Acids. IV. A New Synthetic Approach to Chloramphenicol Base from L-Phenylalanine.
• Studies on Thioamides. I. Synthesis of N-(2-Arylethyl)-thioamides and their Infrared Absorption Spectra.
• The Reductive Cyclization of 1-Methyl-3-aminoalkyloxindoles with Lithium aluminum Hydride.
• Stereochemical Studies. XXXVIII. Asymmetric Synthesis of the Key Compounds for the Synthesis of optically Active Diterpenes. Asymmetric Synthesis of optically Active 1,2,3,4,5,6,7,8,8a-Octahydro-8a-methyl-3,8-naphthalenedione Derivatives with L-Proline De
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• Stereochemical Studies. XXIX. Asymmetric Synthesis of 2-Alkylcyclohexanones via optically Active Lithioenamines
• Stereochemical Studies. XXVIII. Some Aspects of the Asymmetric Synthesis of (R)-(+)-4-Methyl-4-phenyl-2-cyclohexenone via an Enamine
• Stereochemical Studies.XX.Asymmetric Synthesis of α-Bromoketones
• Stereochemical Studies.XIX. Asymmetric Synthesis of 2-Alkyl-4-substituted Cyclohexanones with Enamine Alkylation
• Stereochemical Studies. IX. Asymmetric Synthesis of 2-Alkylcyclo-hexanones with Enamine Alkylation
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• SYNTHESIS OF L-TRYPTOPHAN FROM L-GLUTAMIC ACID
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