1,3-Dipolar cycloadditions of 2-thio-3-chloroacrylamides with diazoalkanes

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TY  - JOUR
  - Kissane, Marie; Lawrence, Simon E; Maguire, Anita R
  - 2010
  - Unknown
  - Organic and Biomolecular Chemistry
  - 1,3-Dipolar cycloadditions of 2-thio-3-chloroacrylamides with diazoalkanes
  - Validated
  - ()
  - 8
  - 1212
  - 2735
  - 2748
  - 2-Thio-3-chloroacrylamides undergo 1,3-dipolar cycloaddns. with diazoalkanes leading to a series of novel pyrazolines and pyrazoles. The mechanistic and synthetic features of the cycloaddns. to the 2-thio-3-chloroacrylamides at both the sulfide and sulfoxide levels of oxidn. are rationalized on the basis of the nature of the substituents.
  - 1477-0520
DA  - 2010/NaN
ER  - 
@article{V57685681,
   = {Kissane, Marie and  Lawrence, Simon E and  Maguire, Anita R},
   = {2010},
   = {Unknown},
   = {Organic and Biomolecular Chemistry},
   = {1,3-Dipolar cycloadditions of 2-thio-3-chloroacrylamides with diazoalkanes},
   = {Validated},
   = {()},
   = {8},
   = {1212},
  pages = {2735--2748},
   = {{2-Thio-3-chloroacrylamides undergo 1,3-dipolar cycloaddns. with diazoalkanes leading to a series of novel pyrazolines and pyrazoles. The mechanistic and synthetic features of the cycloaddns. to the 2-thio-3-chloroacrylamides at both the sulfide and sulfoxide levels of oxidn. are rationalized on the basis of the nature of the substituents.}},
  issn = {1477-0520},
  source = {IRIS}
}
AUTHORSKissane, Marie; Lawrence, Simon E; Maguire, Anita R
YEAR2010
MONTHUnknown
JOURNAL_CODEOrganic and Biomolecular Chemistry
TITLE1,3-Dipolar cycloadditions of 2-thio-3-chloroacrylamides with diazoalkanes
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME8
ISSUE1212
START_PAGE2735
END_PAGE2748
ABSTRACT2-Thio-3-chloroacrylamides undergo 1,3-dipolar cycloaddns. with diazoalkanes leading to a series of novel pyrazolines and pyrazoles. The mechanistic and synthetic features of the cycloaddns. to the 2-thio-3-chloroacrylamides at both the sulfide and sulfoxide levels of oxidn. are rationalized on the basis of the nature of the substituents.
PUBLISHER_LOCATION
ISBN_ISSN1477-0520
EDITION
URL
DOI_LINK
FUNDING_BODY
GRANT_DETAILS