A Highly Stereoselective Synthesis of Glycidic Amides Based on a New Class of Chiral Sulfonium Salts: Applications in Asymmetric Synthesis

2012 ◽  
Vol 18 (47) ◽  
pp. 15190-15201 ◽  
Author(s):  
Francisco Sarabia ◽  
Carlos Vivar-García ◽  
Miguel García-Castro ◽  
Cristina García-Ruiz ◽  
Francisca Martín-Gálvez ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Stereoselective Synthesis ◽  
Sulfonium Salts ◽  
New Class

ChemInform Abstract: A Highly Stereoselective Synthesis of Glycidic Amides Based on a New Class of Chiral Sulfonium Salts: Applications in Asymmetric Synthesis.

ChemInform ◽  
2013 ◽  
Vol 44 (16) ◽  
pp. no-no
Author(s):  
Francisco Sarabia ◽  
Carlos Vivar-Garcia ◽  
Miguel Garcia-Castro ◽  
Cristina Garcia-Ruiz ◽  
Francisca Martin-Galvez ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Stereoselective Synthesis ◽  
Sulfonium Salts ◽  
New Class

scholarly journals Stereoselective synthesis of spirocyclic pyrrolidines/pyrrolizidines/pyrrolothiazolidines using l-proline functionalized manganese ferrite nanorods as a novel heterogeneous catalyst

RSC Advances ◽  
2021 ◽  
Vol 11 (24) ◽  
pp. 14755-14768
Author(s):  
Malihe Akhavan ◽  
Ahmadreza Bekhradnia
Keyword(s):  
Heterogeneous Catalyst ◽  
Stereoselective Synthesis ◽  
Manganese Ferrite ◽  
One Pot ◽  
New Class

An efficient, green, one-pot, and three-component protocol has been reported for the stereoselective synthesis of a new class of spiro thiazolidines.

scholarly journals Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters

2015 ◽  
Vol 51 (43) ◽  
pp. 8939-8941 ◽  
Author(s):  
Sandra Medina ◽  
Alexander S. Henderson ◽  
John F. Bower ◽  
M. Carmen Galan
Keyword(s):  
Room Temperature ◽  
Stereoselective Synthesis ◽  
Co Catalysts ◽  
New Class ◽  
Stereoselective Glycosylation ◽  
Glycosyl Donors

The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoters of trichloroacetimidate glycosyl donors at room temperature is described.

scholarly journals Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry

Molecules ◽  
2020 ◽  
Vol 25 (2) ◽  
pp. 401 ◽  
Author(s):  
Franz Steppeler ◽  
Dominika Iwan ◽  
Elżbieta Wojaczyńska ◽  
Jacek Wojaczyński
Keyword(s):  
Hydrogen Bond ◽  
Drug Development ◽  
Asymmetric Synthesis ◽  
Stereoselective Synthesis ◽  
Strong Hydrogen Bond ◽  
Hydrogen Bond Donor ◽  
Drug Candidates ◽  
Current State ◽  
The Family ◽  
Donor Capability

For almost 20 years, thioureas have been experiencing a renaissance of interest with the emerged development of asymmetric organocatalysts. Due to their relatively high acidity and strong hydrogen bond donor capability, they differ significantly from ureas and offer, appropriately modified, great potential as organocatalysts, chelators, drug candidates, etc. The review focuses on the family of chiral thioureas, presenting an overview of the current state of knowledge on their synthesis and selected applications in stereoselective synthesis and drug development.

ChemInform Abstract: Transition Metal Complexes. A New Class of Catalysts for the Asymmetric Synthesis of α-Amino Acids by Phase-Transfer Alkylation.

ChemInform ◽  
2010 ◽  
Vol 23 (6) ◽  
pp. no-no
Author(s):  
YU. N. BELOKON' ◽  
V. I. MALEEV ◽  
S. O. VIDENSKAYA ◽  
M. B. SAPOROVSKAYA ◽  
V. A. TSYRYAPKIN ◽  
...  
Keyword(s):  
Amino Acids ◽  
Transition Metal ◽  
Metal Complexes ◽  
Asymmetric Synthesis ◽  
Transition Metal Complexes ◽  
Phase Transfer ◽  
New Class

Using a Temporary Silicon Connection in a Highly Stereoselective Synthesis of a New Class of Cyclic Allenylsilanes

Synthesis ◽  
2005 ◽  
pp. 3389-3397
Author(s):  
Liam R. Cox ◽  
Rui Ramalho ◽  
Julien Beignet ◽  
Alexander C. Humphries
Keyword(s):  
Stereoselective Synthesis ◽  
New Class
Sign in / Sign up

Export Citation Format

Share Document