scholarly journals Grubbs Catalysts Immobilized on Merrifield Resin for Metathesis of Leaf Alcohols by using a Convenient Recycling Approach

ChemistryOpen ◽  
2019 ◽  
Vol 8 (1) ◽  
pp. 45-48 ◽  
Author(s):  
Liang Xia ◽  
Tao Peng ◽  
Gang Wang ◽  
Xiaoxue Wen ◽  
Shouguo Zhang ◽  
...  
Keyword(s):  
Grubbs Catalysts ◽  
Merrifield Resin

Neutral Reducing Agents Supported on Merrifield Resin Obtained by Solid Phase Organic Synthesis

Tetrahedron ◽  
2021 ◽  
pp. 132195
Author(s):  
Milagros Aguilar-Martínez ◽  
Judas Tadeo Vargas-Durazo ◽  
Adrián Ochoa-Terán ◽  
Hisila Santacruz-Ortega ◽  
Karen Ochoa Lara ◽  
...  
Keyword(s):  
Organic Synthesis ◽  
Solid Phase ◽  
Reducing Agents ◽  
Solid Phase Organic Synthesis ◽  
Merrifield Resin

Improved Procedure for Routine13C NMR Analysis of Merrifield Resin Bound Molecules

1999 ◽  
Vol 1 (1) ◽  
pp. 25-27 ◽  
Author(s):  
F. Lorgé, ◽  
A. Wagner ◽  
C. Mioskowski
Keyword(s):  
Nmr Analysis ◽  
Merrifield Resin

Integrating the Schrock and Grubbs Catalysts: Ruthenium-Binaphtholate Catalysts for Olefin Metathesis

2010 ◽  
Vol 49 (22) ◽  
pp. 3807-3810 ◽  
Author(s):  
Johanna M. Blacquiere ◽  
Robert McDonald ◽  
Deryn E. Fogg
Keyword(s):  
Olefin Metathesis ◽  
Grubbs Catalysts

Non-nucleophilic base (KHMDS) mediated nucleophilic conversion of Merrifield resin into aminomethyl resin

2001 ◽  
Vol 42 (32) ◽  
pp. 5517-5519 ◽  
Author(s):  
David F.J Sampson ◽  
Robin G Simmonds ◽  
Mark Bradley
Keyword(s):  
Merrifield Resin

Festphasensynthese von Muramyldipeptiden an isomeren Trialkoxybenzylamin-Harzen / Solid Phase Synthesis of Muramyl Dipeptides on Isomeric Trialkoxybenzylamine Resins

1998 ◽  
Vol 53 (7) ◽  
pp. 753-764 ◽  
Author(s):  
Hans-Jürgen Kohlbaua ◽  
Jochen Tschakert ◽  
Raed A. Al-Qawasmeh ◽  
Tanveer Ahmad Nizamì ◽  
Abdul Malik ◽  
...  
Keyword(s):  
Amino Acids ◽  
Trifluoroacetic Acid ◽  
Solid Phase Synthesis ◽  
Solid Phase ◽  
Subsequent Treatment ◽  
Phase Synthesis ◽  
Merrifield Resin

Abstract New isomeric trialkoxybenzylamine resins are developed coupling phthalimidomethyl-3,5-dimethoxyphenols to the Merrifield resin, followed by subsequent treatment with hydrazine. The generated benzylamine function allows DCC coupling w ith the carboxyl function of amino acids and peptides which are removed as amides after treatment with trifluoroacetic acid. These new trialkoxybenzylamine resins allow expeditious syntheses of peptide amides and glycopeptide amides as is demonstrated for muramyl peptides and analogues.

scholarly journals Variable temperature 1H NMR studies on Grubbs catalysts

2008 ◽  
Vol 693 (7) ◽  
pp. 1252-1260 ◽  
Author(s):  
Margaret M. Gallagher ◽  
A. Denise Rooney ◽  
John J. Rooney
Keyword(s):  
1H Nmr ◽  
Variable Temperature ◽  
Nmr Studies ◽  
Grubbs Catalysts
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