@article{
 title = {A general and mild two-step procedure for the synthesis of aryl and heteroaryl sulfonamides from the corresponding iodides},
 type = {article},
 year = {2011},
 keywords = {Acid labile groups,Oxidative chlorination,Sulfonamides,Thiobenzoates},
 pages = {820-823},
 volume = {52},
 websites = {http://ac.els-cdn.com/S0040403910022689/1-s2.0-S0040403910022689-main.pdf?_tid=dd0998fc68dba4b6635d7c6b3fdf92c8&acdnat=1345640971_bf1588dea35480baf642226e58142b2e,http://dx.doi.org/10.1016/j.tetlet.2010.12.050},
 publisher = {Elsevier Ltd.},
 id = {2cb6351a-7c24-3618-ba97-a03bc6e941cb},
 created = {2015-10-07T14:20:51.000Z},
 file_attached = {true},
 profile_id = {64f7fb50-d000-335d-a02d-06c5f340a97a},
 last_modified = {2018-09-03T10:20:45.907Z},
 read = {false},
 starred = {true},
 authored = {true},
 confirmed = {true},
 hidden = {false},
 citation_key = {Ho2011},
 source_type = {Journal Article},
 notes = {<b>From Duplicate 1 (<i>A general and mild two-step procedure for the synthesis of aryl and heteroaryl sulfonamides from the corresponding iodides</i> - Ho, Danny K H; Chan, Lily; Hooper, Alice; Brennan, Paul E)<br/></b><br/>CAPLUS AN 2011:82248(Journal)},
 private_publication = {false},
 abstract = {A mild two-step preparation of aryl and heteroaryl sulfonyl chlorides and sulfonamides from their corresponding iodides is developed. Acid labile functionalities are shown to be stable under both the copper-catalysed coupling and the subsequent oxidative chlorination. © 2010 American Chemical Society.},
 bibtype = {article},
 author = {Ho, Danny K H and Chan, Lily and Hooper, Alice and Brennan, Paul E.},
 doi = {10.1016/j.tetlet.2010.12.050},
 journal = {Tetrahedron Letters},
 number = {7}
}

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