Literature DB >> 11674522

Stereoselective Backbone Modifications of Peptides via Chelate Enolate Claisen Rearrangement.

Uli Kazmaier1, Sabine Maier.   

Abstract

Year:  1999        PMID： 11674522     DOI： 10.1021/jo9904821

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


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  5 in total

1.  Synthesis of Anti-beta-substituted gamma,delta-unsaturated amino acids via Eschenmoser-Claisen rearrangement.

Authors:  Hongchang Qu; Xuyuan Gu; Byoung J Min; Zhihua Liu; Victor J Hruby
Journal:  Org Lett       Date:  2006-09-14       Impact factor: 6.005

2.  Asymmetric synthesis of seven-membered carbocyclic rings via a sequential oxyanionic 5-exo-dig cyclization/claisen rearrangement process. Total synthesis of (-)-frondosin B.

Authors:  Timo V Ovaska; Jonathan A Sullivan; Sami I Ovaska; Jacob B Winegrad; Justin D Fair
Journal:  Org Lett       Date:  2009-06-18       Impact factor: 6.005

3.  Stereoselective terminal functionalization of small peptides for catalytic asymmetric synthesis of unnatural peptides.

Authors:  Keiji Maruoka; Eiji Tayama; Takashi Ooi
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-12       Impact factor: 11.205

4.  Carbanion-accelerated Claisen rearrangements: asymmetric induction with chiral phosphorus-stabilized anions.

Authors:  Scott E Denmark; John E Marlin; G Rajendra
Journal:  J Org Chem       Date:  2012-10-26       Impact factor: 4.354

5.  Synthesis and late stage modifications of Cyl derivatives.

Authors:  Phil Servatius; Uli Kazmaier
Journal:  Beilstein J Org Chem       Date:  2022-02-04       Impact factor: 2.883
  5 in total

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