Literature DB >> 15068087

A multi-component reaction (MCR) approach to the synthesis of highly diverse polymers with polypeptide-like features.

Claude V Robotham1, Christopher Baker, Brian Cuevas, Khalil Abboud, Dennis L Wright.   

Abstract

A new strategy for the combinatorial synthesis of new materials has been developed through the consecutive application of an Ugi 4CC reaction and a ring-opening metathesis polymerization (ROMP) reaction. Norbornenyl aldehydes and carboxylic acids could be used in the Ugi MCR to give highly diverse monomers that were converted to the corresponding polymers by exposure to the second-generation Grubbs' catalyst. These polymers have structural features reminiscent of polypeptides and the process could be extended to the preparation of chiral materials.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 15068087     DOI: 10.1023/b:modi.0000006777.63423.40

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  9 in total

Review 1.  The multicomponent reactions and their libraries for natural and preparative chemistry.

Authors:  I Ugi; S Heck
Journal:  Comb Chem High Throughput Screen       Date:  2001-02       Impact factor: 1.339

2.  Dynamic diversity in drug discovery: Putting small-molecule evolution to work.

Authors: 
Journal:  Drug Discov Today       Date:  2000-02       Impact factor: 7.851

Review 3.  Biomaterials in drug delivery and tissue engineering: one laboratory's experience.

Authors:  R Langer
Journal:  Acc Chem Res       Date:  2000-02       Impact factor: 22.384

4.  The development of L2X2Ru=CHR olefin metathesis catalysts: an organometallic success story.

Authors:  T M Trnka; R H Grubbs
Journal:  Acc Chem Res       Date:  2001-01       Impact factor: 22.384

5.  Highly Efficient Ring-Opening Metathesis Polymerization (ROMP) Using New Ruthenium Catalysts Containing N-Heterocyclic Carbene Ligands C.B. is grateful to the National Science Foundation for a pre-doctoral fellowship. The authors thank Dr. Matthias Scholl for providing catalysts 4 a and 4 c.

Authors: 
Journal:  Angew Chem Int Ed Engl       Date:  2000-08-18       Impact factor: 15.336

6.  Fenchylamine sulfonamide inhibitors of amyloid beta peptide production by the gamma-secretase proteolytic pathway: potential small-molecule therapeutic agents for the treatment of Alzheimer's disease.

Authors:  G M Rishton; D M Retz; P A Tempest; J Novotny; S Kahn; J J Treanor; J D Lile; M Citron
Journal:  J Med Chem       Date:  2000-06-15       Impact factor: 7.446

7.  Increased polymer length of oligopeptide-substituted polynorbornenes with LiCl.

Authors:  Kenny S Roberts; Nicole S Sampson
Journal:  J Org Chem       Date:  2003-03-07       Impact factor: 4.354

8.  Solution phase synthesis of libraries of polycyclic natural product analogues by cascade radical annulation: synthesis of a 64-member library of mappicine analogues and a 48-member library of mappicine ketone analogues.

Authors:  O de Frutos; D P Curran
Journal:  J Comb Chem       Date:  2000 Nov-Dec

9.  Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine.

Authors:  E J Corey; Takanori Shibata; Thomas W Lee
Journal:  J Am Chem Soc       Date:  2002-04-17       Impact factor: 15.419

  9 in total
  1 in total

1.  Direct Catalytic Route to Biomass-Derived 2,5-Furandicarboxylic Acid and Its Use as Monomer in a Multicomponent Polymerization.

Authors:  Oliver R Schade; Patrick-Kurt Dannecker; Kai F Kalz; David Steinbach; Michael A R Meier; Jan-Dierk Grunwaldt
Journal:  ACS Omega       Date:  2019-10-01
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.