Stereoselective synthesis of enantiomerically pure inherently chiral p-tert-butylcalix[4]arene carboxylic acids

[1]  C. Su,et al.  Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis , 2011, International journal of molecular sciences.

[2]  C. Rosini,et al.  Absolute configuration assignment of inherently chiral calix[4]arenes using DFT calculations of chiroptical properties. , 2010, Organic Letters.

[3]  Chuan-Feng Chen,et al.  Synthesis and structures of novel enantiopure inherently chiral calix[4]arene-derived salphen ligands and their transition-metal complexes , 2009 .

[4]  V. Kalchenko,et al.  Proximal heteroalkylation of monoalkoxycalix(4)arenes in synthesis of inherently chiral molecules , 2009 .

[5]  Chuan-Feng Chen,et al.  Inherently chiral calix[4]arene-based bifunctional organocatalysts for enantioselective aldol reactions , 2008 .

[6]  Yong Yang,et al.  Effective nonenzymatic kinetic resolution of racemic m-nitro-substituted inherently chiral aminocalix[4]arenes. , 2008, Organic letters.

[7]  Chuan-feng Chen,et al.  A new approach to enantiopure inherently chiral calix[4]arenes: determination of their absolute configurations. , 2007, Organic letters.

[8]  S. Shimizu,et al.  Design of a novel inherently chiral calix[4]arene for chiral molecular recognition. , 2007, Organic letters.

[9]  V. Kalchenko,et al.  Diastereoselective lower rim (1S)-camphorsulfonylation as the shortest way to the inherently chiral calix[4]arene. , 2007, Organic letters.

[10]  R. Zubatyuk,et al.  A stereoselective synthesis of asymmetrically substituted calix[4]arenecarbamates , 2006 .

[11]  Yan‐Song Zheng,et al.  Chiral nitrogen-containing calix[4]crown—an excellent receptor for chiral recognition of mandelic acid , 2006 .

[12]  A. Demir,et al.  Synthesis and chiral recognition properties of two novel chiral calix[4]arene tartaric ester derivatives , 2006 .

[13]  Chuan-feng Chen,et al.  Synthesis and optical resolution of a series of inherently chiral calix[4]crowns with cone and partial cone conformations. , 2005, Chemistry.

[14]  Jun Luo,et al.  Facile synthesis and optical resolution of inherently chiral fluorescent calix[4]crowns: enantioselective recognition towards chiral leucinol , 2005 .

[15]  Chuan-feng Chen,et al.  Efficient syntheses and resolutions of inherently chiral calix[4]quinolines in the cone and partial-cone conformation. , 2005, The Journal of organic chemistry.

[16]  C. Gaeta,et al.  Synthesis of calix[4]arene derivatives bearing chiral pendant groups as ligands for enantioselective catalysis , 2005 .

[17]  D. Matt,et al.  Bis-phosphites and bis-phosphinites based on distally-functionalised calix[4]arenes: coordination chemistry and use in rhodium-catalysed, low-pressure olefin hydroformylation. , 2005, Dalton Transactions.

[18]  T. Hattori,et al.  Resolution of inherently chiral anti - O , O ′-dialkylated calix[4]arenes and determination of their absolute stereochemistries by CD and X-ray methods , 2005 .

[19]  V. Kalchenko,et al.  Alkylation of narrow rim calix[4]arenes in a DMSO-NaOH medium , 2005 .

[20]  H. Katagiri,et al.  Synthesis of an inherently chiral O,O′-bridged thiacalix[4]crowncarboxylic acid and its application to a chiral solvating agent , 2004 .

[21]  Yan‐Song Zheng,et al.  Exceptional Chiral Recognition of Racemic Carboxylic Acids by Calix[4]arenes Bearing Optically Pure α,β-Amino Alcohol Groups , 2004 .

[22]  Mei-Xiang Wang,et al.  Preparation of both antipodes of enantiopure inherently chiral calix[4]crowns. , 2004, The Journal of organic chemistry.

[23]  Richard I. Cooper,et al.  CRYSTALS version 12: software for guided crystal structure analysis , 2003 .

[24]  F. Sansone,et al.  Novel cinchona carbamate selectors with complementary enantioseparation characteristics for N-acylated amino acids. , 2003, Chirality.

[25]  Xiaojun Wu,et al.  New type chiral calix[4](aza)crowns: synthesis and chiral recognition , 2002 .

[26]  V. Kalchenko,et al.  Symmetrical and inherently chiral water-soluble calix[4]arenes bearing dihydroxyphosphoryl groups , 2002 .

[27]  M. Sugiura,et al.  Lewis acid-catalyzed ring-opening reactions of semicyclic N,O-acetals. , 2001, Organic letters.

[28]  D. Matt,et al.  Diphosphines based on an inherently chiral calix[4]arene scaffold: synthesis and use in enantioselective catalysis , 2001 .

[29]  P. Neri,et al.  Resolution of inherently chiral calix[4]arenes with AABB and CDCD substitution patterns on the upper and lower rims, respectively , 2000 .

[30]  Ishida,et al.  Acid-promoted rearrangement of carbonate functionality anchored to the lower rim of a Calix , 2000, Organic letters.

[31]  Miyano,et al.  Syntheses of chirally modified thiacalix , 2000, Enantiomer.

[32]  Sumio Tokita,et al.  Colorimetric chiral recognition by a molecular sensor , 1996, Nature.

[33]  V. Böhmer,et al.  Calixarenes, Macrocycles with (Almost) Unlimited Possibilities , 1995 .

[34]  S. Shinkai,et al.  Conformations and structures of tetra-O-alkyl-p-tert-butylcalix[4]arenes. How is the conformation of calix[4]arenes immobilized? , 1991 .

[35]  C. Gutsche Calixarenes: An Introduction , 1989 .