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Literature DB >> 11592138

Rational Molecular Design and EPC Synthesis of a Type VI beta-Turn Inducing Peptide Mimetic This work was supported by the BMBF and the Fonds der Chemischen Industrie. EPC=enantiomerically pure compound.

Tobias Hoffmann¹, Harald Lanig, Reiner Waibel, Peter Gmeiner.

Abstract

Year: 2001 PMID： 11592138 DOI： 10.1002/1521-3773(20010917)40:18<3361::aid-anie3361>3.0.co;2-9

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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9 in total

1. Development of small molecules designed to modulate protein-protein interactions.

Authors: Ye Che; Bernard R Brooks; Garland R Marshall
Journal: J Comput Aided Mol Des Date: 2006-04-19 Impact factor: 3.686

2. Route to three-dimensional fragments using diversity-oriented synthesis.

Authors: Alvin W Hung; Alex Ramek; Yikai Wang; Taner Kaya; J Anthony Wilson; Paul A Clemons; Damian W Young
Journal: Proc Natl Acad Sci U S A Date: 2011-04-11 Impact factor: 11.205

3. An analysis of the complementary stereoselective alkylations of imidazolidinone derivatives toward α-quaternary proline-based amino amides.

Authors: Brian J Knight; Erin E Stache; Eric M Ferreira
Journal: Tetrahedron Date: 2015-05-09 Impact factor: 2.457

4. 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

5. (3R,7aS)-3-(TRICHLOROMETHYL)TETRAHYDROPYRROLO[1,2-C]OXAZOL-1(3H)-ONE: AN AIR AND MOISTURE STABLE REAGENT FOR THE SYNTHESIS OF OPTICALLY ACTIVE α-BRANCHED PROLINES.

Authors: Gerald D Artman; Ryan J Rafferty; Robert M Williams; Gregory L Aaron; Matthew M Davis; Kay M Brummond
Journal: Organic Synth Date: 2009-01-01

Rational Molecular Design and EPC Synthesis of a Type VI beta-Turn Inducing Peptide Mimetic This work was supported by the BMBF and the Fonds der Chemischen Industrie. EPC=enantiomerically pure compound.

1. Development of small molecules designed to modulate protein-protein interactions.

2. Route to three-dimensional fragments using diversity-oriented synthesis.

3. An analysis of the complementary stereoselective alkylations of imidazolidinone derivatives toward α-quaternary proline-based amino amides.

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

5. (3R,7aS)-3-(TRICHLOROMETHYL)TETRAHYDROPYRROLO[1,2-C]OXAZOL-1(3H)-ONE: AN AIR AND MOISTURE STABLE REAGENT FOR THE SYNTHESIS OF OPTICALLY ACTIVE α-BRANCHED PROLINES.

6. A mild and efficient approach to enantioenriched α-hydroxyethyl α,β-unsaturated δ-lactams.

7. Stereoselective Synthesis of Quaternary Proline Analogues.

8. Machine learning estimates of natural product conformational energies.

9. Desymmetrization of 7-azabicycloalkenes by tandem olefin metathesis for the preparation of natural product scaffolds.