4.8 Article

Highly Selective Hydroboration of Alkenes, Ketones and Aldehydes Catalyzed by a Well-Defined Manganese Complex

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 46, 页码 14367-14370

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201607579

关键词

alkenes; carbonyl compounds; hydroboration; manganese catalysis; Markovnikov selectivity

资金

  1. American Chemical Society [54247-UNI3]
  2. CUNY Collaborative Research Incentive Program
  3. PSC-CUNY award [69069-0047]
  4. Office for the Advancement of Research
  5. Program for Research Initiatives for Science Majors (PRISM) at John Jay College, CUNY
  6. National Science Foundation (NSF) [CHE-1464543]
  7. NSF [0840444]
  8. Division Of Chemistry
  9. Direct For Mathematical & Physical Scien [1464543] Funding Source: National Science Foundation

向作者/读者索取更多资源

Well-defined manganese complexes based on inexpensive, readily available ligands, 2,2': 6', 2 ''-terpyridine and its derivatives have been prepared and employed for the selective hydroboration of alkenes, ketones and aldehydes. Highly Markovnikov regioselective hydroboration of styrenes as well as excellent chemoselective hydroboration of ketones over alkenes were achieved, for the first time, by an earth-abundant manganese catalyst.

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