Diels-Alder route to norbornane derived vicinal phosphane/borane frustrated Lewis pairs for the metal-free catalytic hydrogenation of α, β-unsaturated ketones-Reference-Cited by-同舟云学术

Diels-Alder route to norbornane derived vicinal phosphane/borane frustrated Lewis pairs for the metal-free catalytic hydrogenation of α, β-unsaturated ketones

Published:2019-10 Issue: Volume:899 Page:120879
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Wölke Christian,Daniliuc Constantin G.,Kehr Gerald^ORCID,Erker Gerhard^ORCID

Funder

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference51 articles.

1. Frustrated Lewis pairs: metal-free hydrogen activation and more;Stephan;Angew. Chem. Int. Ed.,2010

2. Frustrated Lewis pair chemistry: development and perspectives;Stephan;Angew. Chem. Int. Ed.,2015

3. Noninteracting, vicinal frustrated P/B-Lewis pair at the norbornane framework: synthesis, characterization, and reactions;Sajid;J. Am. Chem. Soc.,2013

4. The chemistry of a non-interacting vicinal frustrated phosphane/borane Lewis pair;Elmer;Chem. Eur J.,2017

5. Electronic control of frustrated Lewis pair behavior: chemistry of a geminal alkylidene-bridged per-pentafluorophenylated P/B pair;Rosorius;Organometallics,2011

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