ChemInform Abstract: Catalytic Asymmetric Reductive Acyl Cross-Coupling: Synthesis of Enantioenriched Acyclic α,α-Disubstituted Ketones.

ChemInform ◽  
2013 ◽  
Vol 44 (44) ◽  
pp. no-no
Author(s):  
Alan H. Cherney ◽  
Nathaniel T. Kadunce ◽  
Sarah E. Reisman
Synlett ◽  
2021 ◽  
Author(s):  
Ying-Yeung Yeung ◽  
Jonathan Wong

AbstractOrganobromine compounds are extremely useful in organic synthesis. In this perspective, a focused discussion on some recent advancements in C–Br bond-forming reactions is presented.1 Introduction2 Selected Recent Advances2.1 Catalytic Asymmetric Bromopolycyclization of Olefinic Substrates2.2 Catalytic Asymmetric Intermolecular Bromination2.3 Some New Catalysts and Reagents for Bromination2.4 Catalytic Site-Selective Bromination of Aromatic Compounds2.5 sp3 C–H Bromination via Atom Transfer/Cross-Coupling3 Outlook


2021 ◽  
Author(s):  
F. Wieland Goetzke ◽  
Alexander M. L. Hell ◽  
Lucy van Dijk ◽  
Stephen P. Fletcher

ChemInform ◽  
2015 ◽  
Vol 46 (34) ◽  
pp. no-no
Author(s):  
Shenlin Huang ◽  
Lisa Koetzner ◽  
Chandra Kanta De ◽  
Benjamin List

2004 ◽  
Vol 6 (1) ◽  
pp. 131-133 ◽  
Author(s):  
Steven P. Miller ◽  
Jeremy B. Morgan ◽  
Nepveux ◽  
James P. Morken

2015 ◽  
Vol 17 (4) ◽  
pp. 940-943 ◽  
Author(s):  
Gia L. Hoang ◽  
Zhao-Di Yang ◽  
Sean M. Smith ◽  
Rhitankar Pal ◽  
Judy L. Miska ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Zongbin Jia ◽  
Qi Yang ◽  
Sanzhong Luo

We report herein a catalytic asymmetric dehydrogenative cross-coupling reaction between enones and tertiary amines enabled by synergistic photoredox and chiral primary amine catalysis. The reaction was proposed to proceed via the interception of iminium ion intermediate, in situ generated from photoredox oxidation, by dienamine at α-position, following by isomerization, leading to aza-Morita-Baylis-Hillman-type products with good diastereo- and enantio- selectivity.


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