Wiegmann S, Mattay J. Inherently Chiral Resorcin[4]arenes: A New Concept for Improving the Functionality. Organic Letters. 2011;13(12):3226-3228.A new reactive postion at the upper rim of inherently chiral resorcin[4]arenes was introduced through cleavage of an up to now unreactive methoxy group through the demethylating reagent 9-I-9-BBN. Conservation of the inherent chirality was warranted through the use of a protecting group at the free phenol group
Resorcin[4]arenes represents a class of widely studied macrocycles with remarkable complexing proper...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
Wiegmann S, Neumann B, Stammler H-G, Mattay J. Inherently Chiral Cyano-Substituted Resorcin[4]arene:...
Klaes M, Agena C, Kohler M, et al. First synthesis, isolation and characterization of enantiomerical...
Schiendorfer M, Mattay J. Lower rim functionalized chiral resorc[4]arenes derived from citronellal a...
Agena C, Wolff C, Mattay J. First synthesis, isolation and complete characterization of both enantio...
Paletta M, Klaes M, Neumann B, Stammler H-G, Grimme S, Mattay J. Cavity-extended inherently chiral r...
<p>Chiral diamides and tetramidic resorcin[4]arenes deriving from (<i>R</i>,<i>R</i>)-1,2-diaminocyc...
Klaes M, Neumann B, Stammler H-G, Mattay J. Determination of the absolute configuration of inherentl...
Chiral diamides and tetramidic resorcin[4]arenes deriving from (R,R)-1,2-diaminocyclohexane an...
Schiel C, Hembury GA, Borovkov VV, et al. New insights into the geometry of resorc[4]arenes: Solvent...
The synthesis of enantiomerically pure, distally-bridged resorcinarenes 3 with various R groups (CH3...
New synthetic conditions are described for the fully selective formation of the rctt chair stereoiso...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
Resorcin[4]arenes represents a class of widely studied macrocycles with remarkable complexing proper...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
Wiegmann S, Neumann B, Stammler H-G, Mattay J. Inherently Chiral Cyano-Substituted Resorcin[4]arene:...
Klaes M, Agena C, Kohler M, et al. First synthesis, isolation and characterization of enantiomerical...
Schiendorfer M, Mattay J. Lower rim functionalized chiral resorc[4]arenes derived from citronellal a...
Agena C, Wolff C, Mattay J. First synthesis, isolation and complete characterization of both enantio...
Paletta M, Klaes M, Neumann B, Stammler H-G, Grimme S, Mattay J. Cavity-extended inherently chiral r...
<p>Chiral diamides and tetramidic resorcin[4]arenes deriving from (<i>R</i>,<i>R</i>)-1,2-diaminocyc...
Klaes M, Neumann B, Stammler H-G, Mattay J. Determination of the absolute configuration of inherentl...
Chiral diamides and tetramidic resorcin[4]arenes deriving from (R,R)-1,2-diaminocyclohexane an...
Schiel C, Hembury GA, Borovkov VV, et al. New insights into the geometry of resorc[4]arenes: Solvent...
The synthesis of enantiomerically pure, distally-bridged resorcinarenes 3 with various R groups (CH3...
New synthetic conditions are described for the fully selective formation of the rctt chair stereoiso...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
Resorcin[4]arenes represents a class of widely studied macrocycles with remarkable complexing proper...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...