{"issue":"39","title":"In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins","month":"09","doi":"10.1002/anie.201303528","publication_identifier":{"eissn":["1521-3773"],"issn":["1433-7851"]},"_id":"11959","type":"journal_article","citation":{"ama":"Pieber B, Martinez ST, Cantillo D, Kappe CO. In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins. <i>Angewandte Chemie International Edition</i>. 2013;52(39):10241-10244. doi:<a href=\"https://doi.org/10.1002/anie.201303528\">10.1002/anie.201303528</a>","ista":"Pieber B, Martinez ST, Cantillo D, Kappe CO. 2013. In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins. Angewandte Chemie International Edition. 52(39), 10241–10244.","mla":"Pieber, Bartholomäus, et al. “In Situ Generation of Diimide from Hydrazine and Oxygen: Continuous-Flow Transfer Hydrogenation of Olefins.” <i>Angewandte Chemie International Edition</i>, vol. 52, no. 39, Wiley, 2013, pp. 10241–44, doi:<a href=\"https://doi.org/10.1002/anie.201303528\">10.1002/anie.201303528</a>.","ieee":"B. Pieber, S. T. Martinez, D. Cantillo, and C. O. Kappe, “In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins,” <i>Angewandte Chemie International Edition</i>, vol. 52, no. 39. Wiley, pp. 10241–10244, 2013.","chicago":"Pieber, Bartholomäus, Sabrina Teixeira Martinez, David Cantillo, and C. Oliver Kappe. “In Situ Generation of Diimide from Hydrazine and Oxygen: Continuous-Flow Transfer Hydrogenation of Olefins.” <i>Angewandte Chemie International Edition</i>. Wiley, 2013. <a href=\"https://doi.org/10.1002/anie.201303528\">https://doi.org/10.1002/anie.201303528</a>.","short":"B. Pieber, S.T. Martinez, D. Cantillo, C.O. Kappe, Angewandte Chemie International Edition 52 (2013) 10241–10244.","apa":"Pieber, B., Martinez, S. T., Cantillo, D., &#38; Kappe, C. O. (2013). In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins. <i>Angewandte Chemie International Edition</i>. Wiley. <a href=\"https://doi.org/10.1002/anie.201303528\">https://doi.org/10.1002/anie.201303528</a>"},"article_type":"letter_note","oa_version":"None","scopus_import":"1","publisher":"Wiley","publication_status":"published","volume":52,"author":[{"last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","first_name":"Bartholomäus","full_name":"Pieber, Bartholomäus"},{"last_name":"Martinez","first_name":"Sabrina Teixeira","full_name":"Martinez, Sabrina Teixeira"},{"last_name":"Cantillo","full_name":"Cantillo, David","first_name":"David"},{"last_name":"Kappe","full_name":"Kappe, C. Oliver","first_name":"C. Oliver"}],"extern":"1","language":[{"iso":"eng"}],"page":"10241-10244","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","date_created":"2022-08-24T11:01:47Z","abstract":[{"text":"No catalyst required! A highly efficient, catalyst-free process to generate diimide in situ from hydrazine monohydrate and molecular oxygen for the selective reduction of alkenes has been developed. The use of a gas–liquid segmented flow system allowed safe operating conditions and dramatically enhanced this atom-economical reaction, resulting in short processing times.","lang":"eng"}],"date_updated":"2023-02-21T10:09:21Z","publication":"Angewandte Chemie International Edition","intvolume":"        52","date_published":"2013-09-23T00:00:00Z","article_processing_charge":"No","quality_controlled":"1","day":"23","year":"2013"}