Patents by Inventor Yoshiaki Nakahara

Yoshiaki Nakahara has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20240101760
    Abstract: The present invention relates to a method for producing an acetalization product of an ethylene/vinyl alcohol copolymer by acetalization of an ethylene/vinyl alcohol copolymer, wherein the ethylene/vinyl alcohol copolymer is a porous object.
    Type: Application
    Filed: March 28, 2022
    Publication date: March 28, 2024
    Applicant: KURARAY CO., LTD.
    Inventors: Akio TAKASUGI, Takuro NIIMURA, Atsuhiro NAKAHARA, Yoshiaki ASANUMA
  • Publication number: 20120004457
    Abstract: An object of the present invention is to provide a novel method for producing a peptide utilizing a ligation reaction in which ligation efficiency is excellent and side reactions to other functional groups in the peptide are hard to occur, in comparison with the conventional native chemical ligation methods utilizing the thiol auxiliary group. The present invention provides a method for producing a peptide which comprises a step of causing a first peptide and a second peptide to react in the presence of a reducing agent to obtain a ligated product of the first peptide and the second peptide, wherein the first peptide contains, at the C-terminal end, an amino acid derivative having a thioester group, and the second peptide contains, at the N-terminal end, a serine or threonine derivative having a thiol auxiliary group.
    Type: Application
    Filed: October 6, 2009
    Publication date: January 5, 2012
    Applicant: TOKAI UNIVERSITY EDUCATIONAL SYSTEM
    Inventors: Hironobu Hojo, Yoshiaki Nakahara
  • Publication number: 20110184148
    Abstract: An object of the present invention is to provide a method for synthesizing a peptide thioester by using a compound that can be easily obtained within a relatively short time under conditions in which a side reaction is unlikely to occur. In the present invention, a thioester bond is formed by elongating a peptide chain using N-alkyl cysteine as the C-terminal amino acid according to the Fmoc method, carrying out deprotection, and then causing the peptide bond to undergo N—S transfer to the thiol group of N-alkyl cysteine under weak acidic conditions.
    Type: Application
    Filed: October 5, 2007
    Publication date: July 28, 2011
    Applicant: TOKAI UNIVERSITY EDUCATIONAL SYSTEM
    Inventors: Hironobu Hojo, Yoshiaki Nakahara