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Volumn 3, Issue 2, 2001, Pages 196-204

Polymer-supported glyoxylate and α-imino acetates. Versatile reagents for the synthesis of α-hydroxycarboxylic acid and α-amino acid libraries

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; AMINO ACID; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; GLYOXYLIC ACID DERIVATIVE; HYDROXYACID; IMINE; POLYMER;

EID: 0035293285     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc0000850     Document Type: Article
Times cited : (23)

References (61)
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    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 401
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  • 18
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    • For our preliminary communication, Kobayashi, S.; Akiyama, R.; Kitagawa, H J. Comb. Chem. 2000, 2, 438-440. At almost the same time, the synthesis of polymer-supported glyoxylate has been reported. Schlienger, N.; Bryce, M. R.; Hansen, T. K. Tetrahedron Lett. 2000, 41, 5147-5150. See also, Rademann, J.; Meldal, M.; Bock, K. Chem. Eur. J. 1999, 5, 1218-1225.
    • (2000) J. Comb. Chem. , vol.2 , pp. 438-440
    • Kobayashi, S.1    Akiyama, R.2    Kitagawa, H.3
  • 19
    • 0034709661 scopus 로고    scopus 로고
    • For our preliminary communication, Kobayashi, S.; Akiyama, R.; Kitagawa, H J. Comb. Chem. 2000, 2, 438-440. At almost the same time, the synthesis of polymer-supported glyoxylate has been reported. Schlienger, N.; Bryce, M. R.; Hansen, T. K. Tetrahedron Lett. 2000, 41, 5147-5150. See also, Rademann, J.; Meldal, M.; Bock, K. Chem. Eur. J. 1999, 5, 1218-1225.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 5147-5150
    • Schlienger, N.1    Bryce, M.R.2    Hansen, T.K.3
  • 20
    • 0032893082 scopus 로고    scopus 로고
    • For our preliminary communication, Kobayashi, S.; Akiyama, R.; Kitagawa, H J. Comb. Chem. 2000, 2, 438-440. At almost the same time, the synthesis of polymer-supported glyoxylate has been reported. Schlienger, N.; Bryce, M. R.; Hansen, T. K. Tetrahedron Lett. 2000, 41, 5147-5150. See also, Rademann, J.; Meldal, M.; Bock, K. Chem. Eur. J. 1999, 5, 1218-1225.
    • (1999) Chem. Eur. J. , vol.5 , pp. 1218-1225
    • Rademann, J.1    Meldal, M.2    Bock, K.3
  • 21
    • 0032191522 scopus 로고    scopus 로고
    • The usefulness of the SR-MAS NMR technique for structure determination of resins directly without cleavage from the polymer supports has been demonstrated through development of several useful reactions in the solid phase in our laboratories, (a) Kobayashi, S.; Aoki, Y. Tetrahedron Lett. 1998, 39, 7345-7348.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7345-7348
    • Kobayashi, S.1    Aoki, Y.2
  • 26
    • 0042755177 scopus 로고    scopus 로고
    • The ene reaction of 2-phenylpropene with polymer-supported glyoxylate prepared from 1 under the oxidation condition gave 6a in only 54% yield (cf. Table 2, entry 1).
    • The ene reaction of 2-phenylpropene with polymer-supported glyoxylate prepared from 1 under the oxidation condition gave 6a in only 54% yield (cf. Table 2, entry 1).
  • 27
    • 0043256321 scopus 로고    scopus 로고
    • 1H SR-MAS NMR and IR spectra.
    • 1H SR-MAS NMR and IR spectra.
  • 30
    • 0042253907 scopus 로고    scopus 로고
    • The yield was determined after converting to aminoethanol (11a) by reduction of 7a (Scheme 6).
    • The yield was determined after converting to aminoethanol (11a) by reduction of 7a (Scheme 6).
  • 36
    • 0000369701 scopus 로고    scopus 로고
    • Quite recently, Koot used a 2-chloro-2-(trimethylsilyl)-ethoxyacetate resin as a linker. Koot, W-. J. J. Comb. Chem. 1999, 7, 467-473.
    • (1999) J. Comb. Chem. , vol.7 , pp. 467-473
    • Koot, W.-J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.