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      KCI등재 SCIE SCOPUS

      Synthesis of Silicon Traceless Linker for Solid-Phase Reaction

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      https://www.riss.kr/link?id=A104668266

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      다국어 초록 (Multilingual Abstract)

      The silicon linker is the foremost traceless linker used in solid-phase reactions. Hydrogen fluoride (HF) or trifluoroacetic aicd (TFA) can remove the silicon linker with the silicon atom being replaced by a hydrogen atom. In this experiment, the link...

      The silicon linker is the foremost traceless linker used in solid-phase reactions. Hydrogen fluoride
      (HF) or trifluoroacetic aicd (TFA) can remove the silicon linker with the silicon atom being
      replaced by a hydrogen atom. In this experiment, the linkers 1c and 2d, which are the most
      useful in solid-phase reactions, were synthesized. Linker 1c is composed of seven linearly
      linked carbons and linker 2d includes an oxygen atom in the linear carbon chain to increase
      the solvation capacity. The carboxylic acid component of linker 1c and 2d forms an amide or
      ester bond with resin. The synthesized linkers 1c and 2d could be utilized in constructing a
      chemical compound library that includes indole, benzodiazepine and phenothiazine (aromatic
      ring compounds).

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      참고문헌 (Reference)

      1 "reagents for combinatorial organic synthesis: development of a new o-nitrobenzyl photolabile linker for solid phase synthesis" 60 : 2318-2319, 1995

      2 "Total synthesis of natural estroneand estradiol methyl ethers in extremely high enantiomericpurity via an asymmetric Michael addition to an unsaturatedsulfoxide" 1239-1244, 1986

      3 "Solid-phase synthesis of benzopiperazinones" 63 : 1172-1177, 1998

      4 "Metal-halogenexchange of bromoindoles A route to substituted indoles" 5106-5110, 1986

      5 "Efficient solid-phase synthesis of compounds containing phenylalanine and its derivatives via side-chain attachment to the polymer support" 121 : 8407-8408, 1999

      6 "Application of an almost traceless linker in the synthesis of 2-alkylthiobenzimidazole combinatorial libraries" 4 : 215-219, 1998

      7 "A solid phase tracelesssynthesis of quinoxalinones" 41 : 2835-2838, 2000

      8 "A novelmethod for the rapid parameters of theproducts" 48-49, 1986

      9 "A new method for the preparation of tertiary butyl ethersand esters" 2483-2486, 1988

      10 "A highly acid labile silicon linker for solid phase synthesis" 39 : 897-900, 1998

      1 "reagents for combinatorial organic synthesis: development of a new o-nitrobenzyl photolabile linker for solid phase synthesis" 60 : 2318-2319, 1995

      2 "Total synthesis of natural estroneand estradiol methyl ethers in extremely high enantiomericpurity via an asymmetric Michael addition to an unsaturatedsulfoxide" 1239-1244, 1986

      3 "Solid-phase synthesis of benzopiperazinones" 63 : 1172-1177, 1998

      4 "Metal-halogenexchange of bromoindoles A route to substituted indoles" 5106-5110, 1986

      5 "Efficient solid-phase synthesis of compounds containing phenylalanine and its derivatives via side-chain attachment to the polymer support" 121 : 8407-8408, 1999

      6 "Application of an almost traceless linker in the synthesis of 2-alkylthiobenzimidazole combinatorial libraries" 4 : 215-219, 1998

      7 "A solid phase tracelesssynthesis of quinoxalinones" 41 : 2835-2838, 2000

      8 "A novelmethod for the rapid parameters of theproducts" 48-49, 1986

      9 "A new method for the preparation of tertiary butyl ethersand esters" 2483-2486, 1988

      10 "A highly acid labile silicon linker for solid phase synthesis" 39 : 897-900, 1998

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.96 0.2 1.44
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.07 0.87 0.439 0.05
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