An Efficient Enantioselective Approach to Cyclic β-Amino Acid Derivatives via Olefin Metathesis Reactions

2006 ◽  
Vol 71 (8) ◽  
pp. 3317-3320 ◽  
Author(s):  
Giordano Lesma ◽  
Bruno Danieli ◽  
Alessandro Sacchetti ◽  
Alessandra Silvani
ChemInform ◽  
2006 ◽  
Vol 37 (37) ◽  
Author(s):  
Giordano Lesma ◽  
Bruno Danieli ◽  
Alessandro Sacchetti ◽  
Alessandra Silvani

ChemInform ◽  
2010 ◽  
Vol 30 (2) ◽  
pp. no-no
Author(s):  
S. N. OSIPOV ◽  
C. BRUNEAU ◽  
M. PICQUET ◽  
A. F. KOLOMIETS ◽  
P. H. DIXNEUF

1998 ◽  
pp. 2053-2054 ◽  
Author(s):  
Sergey N. Osipov ◽  
Alexey F. Kolomiets ◽  
Christian Bruneau ◽  
Michel Picquet ◽  
Pierre H. Dixneuf

2017 ◽  
Vol 2017 (14) ◽  
pp. 1894-1901 ◽  
Author(s):  
Márton Kardos ◽  
Loránd Kiss ◽  
Matti Haukka ◽  
Santos Fustero ◽  
Ferenc Fülöp

Synthesis ◽  
2018 ◽  
Vol 50 (18) ◽  
pp. 3571-3588 ◽  
Author(s):  
Loránd Kiss ◽  
Márton Kardos ◽  
Csaba Vass ◽  
Ferenc Fülöp

Because of their biological relevance, cyclic β-amino acids have generated increasing interest and had significant impact in drug research over the past two decades. Their preparation and further functionalization towards new types of molecular entities have received large interest in synthetic and medicinal chemistry. Various types of metathesis reactions, such as ring-opening (ROM), ring-closing (RCM), or cross metathesis (CM) are used widely for access to either alicyclic β-amino acids or other densely functionalized derivatives of this group of compounds. This account intends to provide an insight into the most relevant synthetic routes to this class of derivatives with the application of metathesis reactions. The review focuses on the presentation of selective and stereocontrolled methodologies in view of versatility, robustness, limitations and efficiency.1 Introduction2 Synthesis and Transformation of Cyclic β-Amino Acids through Metathesis Reactions2.1 Synthesis of Five- and Six-Membered Cyclic β-Amino Acids by Ring-Closing Metathesis2.2 Synthesis of Five- and Six-Membered Cyclic β-Amino Acids by Cross Metathesis2.3 Synthesis of β-Amino Acids with Larger Ring Systems by Ring- Closing Metathesis2.4 Synthesis of β-Amino Acids with Condensed Ring Systems by Ring-Rearrangement Metathesis2.5 Stereocontrolled One-Step Synthesis of Functionalized Cispentacin and Transpentacin Derivatives2.5.1 Stereocontrolled Synthesis of Functionalized Cispentacin and Transpentacin Derivatives through Ring-Opening Metathesis of Norbornene β-Amino Acid Derivatives2.5.2 Stereocontrolled Synthesis of Functionalized Azetidinones and β-Amino Acid Derivatives from Condensed Ring β-Lactams by Ring-Opening Metathesis2.5.3 Carbon–Carbon Double Bond Functionalization of β-Amino Acid Derivatives and β-Lactams with α,β-Unsaturated Carbonyl Compounds through Cross Metathesis2.5.4 Synthesis of Functionalized β-Amino Acid Derivatives and β-Lactams through Chemoselective Cross Metathesis3 Conclusions and Outlook


2019 ◽  
Vol 2019 (31-32) ◽  
pp. 5285-5293 ◽  
Author(s):  
Melinda Nonn ◽  
Zsanett Benke ◽  
Santos Fustero ◽  
Ferenc Fülöp ◽  
Loránd Kiss

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