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Volumn , Issue 10, 2009, Pages 1694-1702

One-portion synthesis of 2-acetoxy carbonyl compounds from aldehydes by using an acetylated masked acyl cyanide

Author keywords

2 acetoxy amides; 2 acetoxy esters; Masked acyl cyanide; One portion synthesis; Umpolung

Indexed keywords

2-ACETOXY AMIDES; 2-ACETOXY ESTERS; MASKED ACYL CYANIDE; ONE-PORTION SYNTHESIS; UMPOLUNG;

EID: 67650066281     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1088044     Document Type: Article
Times cited : (17)

References (64)
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    • John Wiley: New York, and references cited therein
    • Hase, T. A. Umpoled Synthons; John Wiley: New York, 1987, and references cited therein.
    • (1987) Umpoled Synthons
    • Hase, T.A.1
  • 17
    • 85166363124 scopus 로고    scopus 로고
    • On the basis on our surveys and consideration, hydrogen cyanide is the only known example of the HC?Y6 type. Thus, recently reported Strecker reactions are cited: (a) Iyer, M. S, Gigstad, K. M, Namdev, N. D, Lipton, M. J. Am. Chem. Soc. 1996, 118, 4910
    • 6 type. Thus, recently reported Strecker reactions are cited: (a) Iyer, M. S.; Gigstad, K. M.; Namdev, N. D.; Lipton, M. J. Am. Chem. Soc. 1996, 118, 4910.
  • 26
    • 67650051449 scopus 로고    scopus 로고
    • General structure 1 is from reference 3i.
    • General structure 1 is from reference 3i.
  • 27
    • 0342802320 scopus 로고    scopus 로고
    • Although the term 'masked acyl cyanide' was mentioned in the following paper, generation of an 'unmasked acyl cyanide' was unsuccessful: Khatri, H. N, Walborsky, H. M. J. Org. Chem. 1978, 43, 734
    • Although the term 'masked acyl cyanide' was mentioned in the following paper, generation of an 'unmasked acyl cyanide' was unsuccessful: Khatri, H. N.; Walborsky, H. M. J. Org. Chem. 1978, 43, 734.
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    • Preparation of 15 and 16: Nemoto, H.; Li, X.; Ma, R.; Suzuki, I.; Shibuya, M. Tetrahedron Lett. 2002, 44, 73.
    • Preparation of 15 and 16: Nemoto, H.; Li, X.; Ma, R.; Suzuki, I.; Shibuya, M. Tetrahedron Lett. 2002, 44, 73.
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    • The following are recent reviews of Ugi and Passerini reactions: (a) Bienaymé, H.; Hulme, C.; Oddon, G.; Schmitt, P. Chem. Eur. J. 2000, 6, 3321.
    • The following are recent reviews of Ugi and Passerini reactions: (a) Bienaymé, H.; Hulme, C.; Oddon, G.; Schmitt, P. Chem. Eur. J. 2000, 6, 3321.
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    • 59049090575 scopus 로고    scopus 로고
    • A total synthesis of Tamiflu using commercially available H-MAC-Ac has been reported: Yamatsigu, K.; Yin, L.; Kamijo, S.; Kimura, Y.; Kanai, M.; Shibasaki, M. Angew. Chem. Int. Ed. 2008, 48, 1070.
    • A total synthesis of Tamiflu using commercially available H-MAC-Ac has been reported: Yamatsigu, K.; Yin, L.; Kamijo, S.; Kimura, Y.; Kanai, M.; Shibasaki, M. Angew. Chem. Int. Ed. 2008, 48, 1070.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.