ChemInform Abstract: Recent Advances in the Generation of Non-Racemic Ferrocene Derivatives and Their Application to Asymmetric Synthesis

ChemInform ◽  
2010 ◽  
Vol 29 (44) ◽  
pp. no-no
Author(s):  
C. J. RICHARDS ◽  
A. J. LOCKE
Keyword(s):  
Asymmetric Synthesis ◽  
Ferrocene Derivatives ◽  
Recent Advances

Enantioselective Functionalization of Prochiral Cyclobutanones and Cyclobutenones

Synlett ◽  
2021 ◽  
Author(s):  
Memg Wang ◽  
Changxu Zhong ◽  
Ping Lu
Keyword(s):  
Asymmetric Synthesis ◽  
Membered Ring ◽  
Enantioselective Synthesis ◽  
Ring Compounds ◽  
Recent Advances ◽  
Cyclobutane Derivatives

Enantioselective synthesis of cyclobutane derivatives is still a challenging topic in asymmetric synthesis. [2+2]-Cycloaddition and skeleton rearrangement are two primary strategies to this end. Recently, functionalization of cyclobutanones and cyclobutenones, which are readily available via [2+2]-cycloadditions as prochiral substrates, has emerged as a powerful tool to access versatile four-membered ring compounds. Herein, we summarize some recent advances in these areas from our and other groups.

scholarly journals Recent Advances in Organocatalyzed Asymmetric Synthesis of Benzopyran and Benzodihydropyran (Chromane) Nuclei

Symmetry ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1510
Author(s):  
Renato Dalpozzo ◽  
Raffaella Mancuso
Keyword(s):  
Natural Products ◽  
Asymmetric Synthesis ◽  
Organic Synthesis ◽  
Building Blocks ◽  
Core Structure ◽  
The Core ◽  
Recent Advances ◽  
Set Up

Benzopyran and benzodihydropyran (chromane) nuclei are the core structure of many natural products, in particular flavonoids. Many compounds possessing this structure are nutraceuticals, pharmaceutical nutrients. Therefore, benzopyran and chromane scaffolds are important building blocks in organic synthesis and many efforts have been made to set up efficient methods for their synthesis. In particular, asymmetric methods are of great importance, being natural products, and generally chiral substances. This review aims to cover literature in the range 2017–first half of 2019.

ChemInform Abstract: Recent Advances in the Catalytic Asymmetric Synthesis of β-Amino Acids

ChemInform ◽  
2010 ◽  
Vol 41 (36) ◽  
pp. no-no
Author(s):  
Barbara Weiner ◽  
Wiktor Szymanski ◽  
Dick B. Janssen ◽  
Adriaan J. Minnaard ◽  
Ben L. Feringa
Keyword(s):  
Amino Acids ◽  
Asymmetric Synthesis ◽  
Catalytic Asymmetric Synthesis ◽  
Recent Advances ◽  
Catalytic Asymmetric

Chiral 1,3,2-Oxazaborolidines in Asymmetric Synthesis: Recent Advances

ChemInform ◽  
2004 ◽  
Vol 35 (52) ◽  
Author(s):  
V. A. Glushkov ◽  
A. G. Tolstikov
Keyword(s):  
Asymmetric Synthesis ◽  
Recent Advances

Recent advances in asymmetric synthesis with CO2

2020 ◽  
Vol 63 (10) ◽  
pp. 1336-1351 ◽  
Author(s):  
Chuan-Kun Ran ◽  
Xiao-Wang Chen ◽  
Yong-Yuan Gui ◽  
Jie Liu ◽  
Lei Song ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Recent Advances

Iridium-Catalyzed Asymmetric C–H Borylation Enabled by Chiral Bidentate Boryl Ligands

Synlett ◽  
2019 ◽  
Vol 30 (19) ◽  
pp. 2107-2112 ◽  
Author(s):  
Yongjia Shi ◽  
Qian Gao ◽  
Senmiao Xu
Keyword(s):  
Drug Discovery ◽  
Asymmetric Synthesis ◽  
Synthetic Chemistry ◽  
Organoboron Compounds ◽  
Recent Advances ◽  
Optically Pure

Asymmetric synthesis of optically pure organoboron compounds is a topic that has received a number of attentions owing to their particular importance in synthetic chemistry and drug discovery. We herein highlight recent advances in the iridium-catalyzed C–H borylation of diarylmethylamines and cyclopropanes enabled by chiral bidentate boryl ligands.1 Introduction2 Ir-Catalyzed Asymmetric C(sp2)–H Borylation of Diarylmethylamines3 Ir-Catalyzed Enantioselective C(sp3)–H Borylation of Cyclopropanes4 Conclusion

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