IRIS publication 57685681
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 -
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@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} }
Data as stored in IRIS
AUTHORS | Kissane, Marie; Lawrence, Simon E; Maguire, Anita R | ||
YEAR | 2010 | ||
MONTH | Unknown | ||
JOURNAL_CODE | Organic and Biomolecular Chemistry | ||
TITLE | 1,3-Dipolar cycloadditions of 2-thio-3-chloroacrylamides with diazoalkanes | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
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VOLUME | 8 | ||
ISSUE | 1212 | ||
START_PAGE | 2735 | ||
END_PAGE | 2748 | ||
ABSTRACT | 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. | ||
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ISBN_ISSN | 1477-0520 | ||
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