ChemInform Abstract: A New Method for the One-Pot Synthesis of α-Hydroxyaldehyde Ethyl Sulfates from Terminal Olefins.

ChemInform ◽  
2010 ◽  
Vol 27 (52) ◽  
pp. no-no
Author(s):  
N. V. ZYK ◽  
E. E. NESTEROV ◽  
A. N. KHLOBYSTOV ◽  
N. S. ZEFIROV
Keyword(s):  
New Method ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One ◽  
Terminal Olefins

scholarly journals New sulfuryl fluoride-derived alkylating reagents for the 1,1-dihydrofluoroalkylation of thiols

2019 ◽  
Vol 10 (44) ◽  
pp. 10331-10335 ◽  
Author(s):  
Paul J. Foth ◽  
Frances Gu ◽  
Trevor G. Bolduc ◽  
Sahil S. Kanani ◽  
Glenn M. Sammis
Keyword(s):  
New Method ◽  
One Pot ◽  
Sulfuryl Fluoride ◽  
One Pot Synthesis ◽  
The One ◽  
Alkylating Reagents

Herein, we report a new method for the one-pot synthesis of 1,1-dihydrofluoroalkyl sulfides by bubbling sulfuryl fluoride (SO2F2) through a solution of the corresponding alcohol and thiol.

Intermolecular sp 3 C–H bond functionalization of alkyl amides as a new method for the one-pot synthesis of functional neo alkyl amides with remote functional groups

2015 ◽  
Vol 56 (3) ◽  
pp. 562-566 ◽  
Author(s):  
Irena S. Akhrem ◽  
Dzhul’etta V. Avetisyan ◽  
Lyudmila V. Afanas’eva ◽  
Oleg I. Artyushin ◽  
Nikolai D. Kagramanov
Keyword(s):  
Functional Groups ◽  
New Method ◽  
One Pot ◽  
Bond Functionalization ◽  
One Pot Synthesis ◽  
The One

A new method for α-specific glucosylation and its application to the one-pot synthesis of a branched α-glucan

2019 ◽  
Vol 6 (6) ◽  
pp. 762-772 ◽  
Author(s):  
Yanxin Zhang ◽  
Shihao Zhou ◽  
Xiaohan Wang ◽  
Han Zhang ◽  
Zhongwu Guo ◽  
...  
Keyword(s):  
New Method ◽  
Protecting Groups ◽  
One Pot ◽  
Highly Efficient ◽  
One Pot Synthesis ◽  
The One ◽  
Remote Participation ◽  
Promoter System

We have developed a new and highly efficient α-specific glucosylation method based on the synergistic α-directing effects of a TolSCl/AgOTf promoter system and the steric β-shielding or the remote participation of protecting groups at the donor 6-O-position.

Intermolecular sp3 C–H bond functionalization of alkyl alkanoates as a new method for the one-pot synthesis of functional neo alkyl alkanoates with remote functional groups

2013 ◽  
Vol 54 (45) ◽  
pp. 6037-6040 ◽  
Author(s):  
Irena S. Akhrem ◽  
Dzhul’etta V. Avetisyan ◽  
Irina M. Churilova ◽  
Lyudmila V. Afanas’eva ◽  
Oleg I. Artyushin ◽  
...  
Keyword(s):  
Functional Groups ◽  
New Method ◽  
One Pot ◽  
Bond Functionalization ◽  
One Pot Synthesis ◽  
The One

An Overview of the One-pot Synthesis of Imidazolines

2020 ◽  
Vol 24 (20) ◽  
pp. 2341-2355
Author(s):  
Thaipparambil Aneeja ◽  
Sankaran Radhika ◽  
Mohan Neetha ◽  
Gopinathan Anilkumar
Keyword(s):  
Asymmetric Catalysis ◽  
Organic Compounds ◽  
Ring Opening ◽  
Ecological Impact ◽  
Chiral Auxiliary ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One ◽  
Synthetic Intermediate ◽  
Heterocyclic Moiety

One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.

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