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Volumn 13, Issue 11, 2011, Pages 2810-2813

Enantioselective iridium-catalyzed allylic substitutions with hydroxamic acid derivatives as N-nucleophiles

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EID: 79957823107     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200688d     Document Type: Article
Times cited : (39)

References (46)
  • 1
    • 38049017956 scopus 로고    scopus 로고
    • Reviews covering the whole field
    • Reviews covering the whole field: Lu, Z.; Ma, S. Angew. Chem., Int. Ed. 2008, 47, 258-297
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 258-297
    • Lu, Z.1    Ma, S.2
  • 24
    • 79957822925 scopus 로고    scopus 로고
    • The assignment of the absolute configuration is based on a rule on the configurational course of the Ir-catalyzed allylic substitution, which was always found valid so far (ref 2).
    • The assignment of the absolute configuration is based on a rule on the configurational course of the Ir-catalyzed allylic substitution, which was always found valid so far (ref 2).
  • 25
    • 79957834684 scopus 로고    scopus 로고
    • It is very important that this compound be carefully dried (see Supporting Information).
    • It is very important that this compound be carefully dried (see Supporting Information).
  • 33
    • 79957849413 scopus 로고    scopus 로고
    • The assignment of the relative configuration of 7 is tentative.
    • The assignment of the relative configuration of 7 is tentative.
  • 45
    • 79957819792 scopus 로고    scopus 로고
    • The feasibility of Weinreb type chemistry was checked with amide 8. Upon addition of DIBAL-H at -78 °C the deacylation product, N -{(1 S)-1-[(benzyloxy)methyl]prop-2-en-1-yl}- O -methylhydroxylamine (4e ), was isolated in 96% yield.
    • The feasibility of Weinreb type chemistry was checked with amide 8. Upon addition of DIBAL-H at -78 °C the deacylation product, N -{(1 S)-1-[(benzyloxy)methyl]prop-2-en-1-yl}- O -methylhydroxylamine (4e ), was isolated in 96% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.