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Volumn 41, Issue 5, 2000, Pages 591-594

Expeditious amide-forming reactions using thiol esters

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; THIOESTER;

EID: 0034728203     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)02132-2     Document Type: Article
Times cited : (15)

References (24)
  • 16
    • 0014784491 scopus 로고
    • All arylthiol esters described in this communication were prepared from tributylphosphine and aryl disulfide in the presence of the carboxylic acid in THF at rt. See
    • All arylthiol esters described in this communication were prepared from tributylphosphine and aryl disulfide in the presence of the carboxylic acid in THF at rt. See: Mukaiyama, T.; Matsuda, R.; Suzuki, M. Tetrahedron Lett. 1970, 1901.
    • (1970) Tetrahedron Lett. , pp. 1901
    • Mukaiyama, T.1    Matsuda, R.2    Suzuki, M.3
  • 17
    • 0015522445 scopus 로고
    • The abbreviations for amino acids follow the IUPAC-IUB Joint Commission on Biochemistry Nomenclature
    • The abbreviations for amino acids follow the IUPAC-IUB Joint Commission on Biochemistry Nomenclature: J. Biol. Chem. 1971, 247, 977.
    • (1971) J. Biol. Chem. , vol.247 , pp. 977
  • 18
    • 0343222673 scopus 로고    scopus 로고
    • The esterification reactions of tolylthiol ester with secondary or tertiary alcohols are approximately two times faster than those of benzenethiol ester with silver trifluoroacetate. These results indicate that alkyl substitution in para position of aryl group enhances the reactivity toward the thiophilic reagents
    • The esterification reactions of tolylthiol ester with secondary or tertiary alcohols are approximately two times faster than those of benzenethiol ester with silver trifluoroacetate. These results indicate that alkyl substitution in para position of aryl group enhances the reactivity toward the thiophilic reagents.
  • 19
    • 0342788060 scopus 로고    scopus 로고
    • 1H NMR
    • 1H NMR.
  • 21
    • 0025014543 scopus 로고
    • An acid chloride method has been used to form peptide linkages with N-hydroxy-α-amino acid derivatives at an elevated temperature. see: (a)
    • An acid chloride method has been used to form peptide linkages with N-hydroxy-α-amino acid derivatives at an elevated temperature. see: (a) Durette, P. L.; Baker, F.; Baker, P. L.; Boger, J.; Bondy, S. S.; Hammond, M. L.; Lanza, T. J.; Pessolano, A. A.; Caldwell, C. G. Tetrahedron Lett. 1990, 31, 1237.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1237
    • Durette, P.L.1    Baker, F.2    Baker, P.L.3    Boger, J.4    Bondy, S.S.5    Hammond, M.L.6    Lanza, T.J.7    Pessolano, A.A.8    Caldwell, C.G.9
  • 23
    • 0342788059 scopus 로고    scopus 로고
    • BOP=benzotriazole-1-yloxytripyrrolidinophosphonium hexafluorophosphate
    • BOP=benzotriazole-1-yloxytripyrrolidinophosphonium hexafluorophosphate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.