Chiral reagents in glycosylation and modification of carbohydrates

2018 ◽  
Vol 47 (3) ◽  
pp. 681-701 ◽  
Author(s):  
Hao-Yuan Wang ◽  
Stephanie A. Blaszczyk ◽  
Guozhi Xiao ◽  
Weiping Tang

This review summarizes recent advances in stereoselective glycosylation and site-selective functionalization of carbohydrates mediated by chiral reagents including chiral auxiliaries and chiral catalysts.

2019 ◽  
Vol 471 ◽  
pp. 64-77 ◽  
Author(s):  
Stephanie A. Blaszczyk ◽  
Timothy C. Homan ◽  
Weiping Tang

2021 ◽  
Author(s):  
Qi Zhang ◽  
Bing-Feng Shi

Recent advances in site-selective functionalization of remote aliphatic C–H bonds in organometallic pathways are summarized.


2019 ◽  
Author(s):  
Sandeep Pimparkar ◽  
Trisha Bhattacharya ◽  
Arun Maji ◽  
Argha Saha ◽  
Ramasamy Jayarajan ◽  
...  

The significance of site selective functionalization stands upon the superior selectivity, easy synthesis and diverse product utility. In this work we demonstrate the <i>para</i>-selective introduction of versatile nitrile moiety, enabled by detachable and reusable H-bonded auxiliary. The methodology holds its efficiency irrespective of substrate electronic bias. The conspicuous shift in the step energetics was probed by both experimental and computational mechanistic tools heralds the inception of <i>para</i>-deuteration. The synthetic impact of the methodology was highlighted with reusability of directing group and post synthetic modifications


2019 ◽  
Author(s):  
Sandeep Pimparkar ◽  
Trisha Bhattacharya ◽  
Arun Maji ◽  
Argha Saha ◽  
Ramasamy Jayarajan ◽  
...  

The significance of site selective functionalization stands upon the superior selectivity, easy synthesis and diverse product utility. In this work we demonstrate the <i>para</i>-selective introduction of versatile nitrile moiety, enabled by detachable and reusable H-bonded auxiliary. The methodology holds its efficiency irrespective of substrate electronic bias. The conspicuous shift in the step energetics was probed by both experimental and computational mechanistic tools heralds the inception of <i>para</i>-deuteration. The synthetic impact of the methodology was highlighted with reusability of directing group and post synthetic modifications


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


2005 ◽  
Vol 44 (6) ◽  
pp. 947-949 ◽  
Author(s):  
Jin-Hwan Kim ◽  
Hai Yang ◽  
Geert-Jan Boons

2018 ◽  
Vol 9 (1) ◽  
pp. 22-32 ◽  
Author(s):  
Koji Hirano ◽  
Masahiro Miura

This minireview focuses on recent advances in site-selective C–H functionalization on 2-pyridone which is an important heterocyclic motif in medicinal and pharmaceutical chemistry.


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