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Volumn , Issue 10, 2007, Pages 1559-1565

Novel synthesis of arylethynyl heterocycles

Author keywords

Acetylenes; Elimination; Indole; Pyrrole; Tosyl protecting group

Indexed keywords

ELIMINATION; INDOLES; PYRROLES; TOSYL PROTECTING GROUPS;

EID: 34249795443     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-966041     Document Type: Article
Times cited : (14)

References (22)
  • 7
    • 0010653530 scopus 로고    scopus 로고
    • Several procedures have been described for the removal of the protecting group, see: a, Thomas, E. J, Ed, Thieme: Stuttgart
    • Several procedures have been described for the removal of the protecting group, see: (a) Joule, J. A. In Science of Synthesis, Vol. 10; Thomas, E. J., Ed.; Thieme: Stuttgart, 2000, 361.
    • (2000) Science of Synthesis , vol.10 , pp. 361
    • Joule, J.A.1
  • 13
    • 34249808875 scopus 로고    scopus 로고
    • Several procedures can be found in: Tyrrell, E. Alkynes, In Comprehensive Organic Functional Group Transformations II, 1; Katritzky, A. R.; Richard, J. K., Eds.; Elsevier Ltd.: Oxford, 2005, 1083.
    • Several procedures can be found in: Tyrrell, E. Alkynes, In Comprehensive Organic Functional Group Transformations II, Vol. 1; Katritzky, A. R.; Richard, J. K., Eds.; Elsevier Ltd.: Oxford, 2005, 1083.
  • 21
    • 34249785724 scopus 로고    scopus 로고
    • 2O, 0.045%, B: TFA-MeCN, 0.036%. A linear gradient from 50% B to 100% B over 15 minutes was used. The retention times of 1 and 3 were 9.1 and 8.4 min, respectively.
    • 2O, 0.045%, B: TFA-MeCN, 0.036%. A linear gradient from 50% B to 100% B over 15 minutes was used. The retention times of 1 and 3 were 9.1 and 8.4 min, respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.