scholarly journals Highly efficient chemoenzymatic synthesis and facile purification of α-Gal pentasaccharyl ceramide Galα3nLc4βCer

2017 ◽  
Vol 53 (59) ◽  
pp. 8280-8283 ◽  
Author(s):  
Abhishek Santra ◽  
Yanhong Li ◽  
Hai Yu ◽  
Teri J. Slack ◽  
Peng George Wang ◽  
...  
Keyword(s):  
Chemoenzymatic Synthesis ◽  
One Pot ◽  
Highly Efficient

α-Gal pentasaccharyl ceramide was synthesized using sequential one-pot multienzyme (OPME) systems with facile purification using a C18 cartridge followed by acylation.

scholarly journals One-pot chemoenzymatic synthesis of trolline and tetrahydroisoquinoline analogues

2018 ◽  
Vol 54 (11) ◽  
pp. 1323-1326 ◽  
Author(s):  
Jianxiong Zhao ◽  
Benjamin R. Lichman ◽  
John M. Ward ◽  
Helen C. Hailes
Keyword(s):  
Natural Product ◽  
Chemoenzymatic Synthesis ◽  
One Pot ◽  
Highly Efficient

A highly efficient one-pot asymmetric route to tetrahydroisoquinoline alkaloids including the natural product trolline is described.

A One-Pot Chemoenzymatic Synthesis of (2S,4R)-4-Methylproline Enables the First Total Synthesis of Antiviral Lipopeptide Cavinafungin B

2018 ◽  
Author(s):  
Christian R. Zwick ◽  
Hans Renata
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Complex Molecule ◽  
Molecular Target ◽  
Chemoenzymatic Synthesis ◽  
General Strategy ◽  
One Pot

We report an efficient ten-step synthesis of antiviral natural product cavinafungin B in 37% overall yield. By leveraging a one-pot chemoenzymatic synthesis of (2S,4R)-4-methylproline and oxazolidine-tethered (Rink-Boc-ATG-resin) SPPS methodology, the assembly of our molecular target could be conducted in an efficient manner.This general strategy could prove amenable to the construction of other natural and unnatural linear lipopeptides. The value of incorporating biocatalytic steps in complex molecule synthesis is highlighted by this work.

Green and Highly Efficient One-Pot Synthesis of Some New Bis Thiazolidinones

2013 ◽  
Vol 10 (10) ◽  
pp. 764-769 ◽  
Author(s):  
Akbar Mobinikhaledi ◽  
Alireza Amiri
Keyword(s):  
One Pot ◽  
Highly Efficient ◽  
One Pot Synthesis

Iodine Catalyzed Highly Efficient One Pot Three Component Synthesis of 4-arylidene-3-methylisoxazol-5 (4H) -one in Aqueous Medium

2018 ◽  
Vol 5 (2) ◽  
pp. 122-128 ◽  
Author(s):  
Srinivas L. Nakkalwar ◽  
Shivaji B. Patwari ◽  
Mohasim M. Patel ◽  
Vivekanand B. Jadhav
Keyword(s):  
Aqueous Medium ◽  
One Pot ◽  
Highly Efficient

A highly efficient and green approach for the synthesis of pyrimido[4,5-b]quinolines using N,N-diethyl-N-sulfoethanaminium chloride

2021 ◽  
Vol 76 (2) ◽  
pp. 85-90
Author(s):  
Abdolkarim Zare ◽  
Manije Dianat
Keyword(s):  
Reaction Times ◽  
Solvent Free ◽  
One Pot ◽  
Catalyst Amount ◽  
Green Protocol ◽  
Highly Efficient ◽  
Green Approach ◽  
Solvent Free Conditions ◽  
The One ◽  
High Yields

Abstract A highly efficient and green protocol for the synthesis of pyrimido[4,5-b]quinolines has been described. The one-pot multicomponent reaction of dimedone with arylaldehydes and 6-amino-1,3-dimethyluracil in the presence of N,N-diethyl-N-sulfoethanaminium chloride ([Et3N–SO3H][Cl]) as an ionic liquid (IL) catalyst under solvent-free conditions afforded the mentioned compounds in high yields and short reaction times. Our protocol is superior to many of the reported protocols in terms of two or more of these factors: the reaction times, yields, conditions (solvent-free versus usage of organic solvents), temperature and catalyst amount.

Highly efficient protocol for one-pot N-alkylation of nucleobases using alcohols in bmim[Br]: a rapid route to access acyclic nucleosides

2015 ◽  
Vol 12 (9) ◽  
pp. 1603-1612 ◽  
Author(s):  
Mohammad Navid Soltani Rad ◽  
Somayeh Behrouz ◽  
Elham Zarenezhad ◽  
Narjes Kaviani
Keyword(s):  
One Pot ◽  
Highly Efficient ◽  
Acyclic Nucleosides

Fast and highly efficient one-pot synthesis of polyoxadiazole/carbon nanotube nanocomposites in mild acid

2010 ◽  
Vol 60 (3) ◽  
pp. 517-528 ◽  
Author(s):  
Marcio R Loos ◽  
Volker Abetz ◽  
Karl Schulte
Keyword(s):  
Carbon Nanotube ◽  
One Pot ◽  
Highly Efficient ◽  
One Pot Synthesis ◽  
Mild Acid

The first peripherally masked thiol dendrimers: a facile and highly efficient functionalization strategy of polyester dendrimers via one-pot xanthate deprotection/thiol–acrylate Michael addition reactions

2014 ◽  
Vol 50 (50) ◽  
pp. 6574-6577 ◽  
Author(s):  
Sam E. R. Auty ◽  
Oliver Andrén ◽  
Michael Malkoch ◽  
Steven P. Rannard
Keyword(s):  
Michael Addition ◽  
Addition Reactions ◽  
One Pot ◽  
Highly Efficient

We present the first xanthate surface functional dendrimers which undergo rapid one-pot deprotection to thiols and subsequent acrylate Michael addition .

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