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Volumn 75, Issue 15, 2010, Pages 5371-5374

Synthesis of guanidines from azides: A general and straightforward methodology in carbohydrate chemistry

Author keywords

[No Author keywords available]

Indexed keywords

BENZYL ETHERS; CARBOHYDRATE CHEMISTRY; EFFICIENT METHOD; FREE AMINES; GUANIDINE DERIVATIVE; IN-SITU; ONE POT; PROTECTING GROUP; SUBSTITUTION PATTERNS;

EID: 77955167910     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100876r     Document Type: Article
Times cited : (15)

References (55)
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    • Magano, J. Chem. Rev. 2009, 109, 4398-4438
    • (2009) Chem. Rev. , vol.109 , pp. 4398-4438
    • Magano, J.1
  • 31
    • 70350666648 scopus 로고    scopus 로고
    • For other guanidinylating reagents, see
    • For other guanidinylating reagents, see: Wojciechowski, F.; Hudson, R. H. E. Org. Lett. 2009, 11, 4878-4881
    • (2009) Org. Lett. , vol.11 , pp. 4878-4881
    • Wojciechowski, F.1    Hudson, R.H.E.2
  • 34
    • 67649386488 scopus 로고    scopus 로고
    • For substituted guanidines, a Mitsunobu route can also be used. See
    • For substituted guanidines, a Mitsunobu route can also be used. See: Swamy, K. C. K.; Kumar, N. N. B.; Balaraman, E.; Kumar, K. V.P. P. Chem. Rev. 2009, 109, 2551-2651
    • (2009) Chem. Rev. , vol.109 , pp. 2551-2651
    • Swamy, K.C.K.1    Kumar, N.N.B.2    Balaraman, E.3    Kumar, K.V.P.P.4
  • 52
    • 0029034347 scopus 로고
    • For selective inhibition of benzyl ether hydrogenolysis, see
    • For selective inhibition of benzyl ether hydrogenolysis, see: Sajiki, H. Tetrahedron Lett. 1995, 36, 3465-3468
    • (1995) Tetrahedron Lett. , vol.36 , pp. 3465-3468
    • Sajiki, H.1
  • 53
    • 0035859333 scopus 로고    scopus 로고
    • For a similar result, see
    • For a similar result, see: White, R. D.; Wood, J. L. Org. Lett. 2001, 3, 1825-1827
    • (2001) Org. Lett. , vol.3 , pp. 1825-1827
    • White, R.D.1    Wood, J.L.2
  • 55
    • 77955126125 scopus 로고    scopus 로고
    • The use of protected thioureas with the Mukaiyama reagent seems to be superior for guanidinylation of sterically hindered and less reactive amines; see:; Wiley: New York,; Collect. Vol., p
    • The use of protected thioureas with the Mukaiyama reagent seems to be superior for guanidinylation of sterically hindered and less reactive amines; see: Organic Syntheses; Wiley: New York, 2004; Collect. Vol. X, p 266.
    • (2004) Organic Syntheses , vol.10 , pp. 266


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.