Literature DB >> 17487911

Synthesis and stereochemical assignment of FR252921, a promising immunosuppressant.

J Russell Falck1, Anyu He, Hiroki Fukui, Hideyuki Tsutsui, Akella Radha.   

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Year:  2007        PMID: 17487911     DOI: 10.1002/anie.200700321

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


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  5 in total

1.  An enantioselective synthesis of the C3-C21 segment of the macrolide immunosuppressive agent FR252921.

Authors:  Arun K Ghosh; Samuel Rodriguez
Journal:  Tetrahedron Lett       Date:  2016-05-18       Impact factor: 2.415

2.  Tandem Electrocyclic Ring Opening/Radical Cyclization: Application to the Total Synthesis of Cribrostatin 6.

Authors:  Daniel Knueppel; Stephen F Martin
Journal:  Tetrahedron       Date:  2011-12-23       Impact factor: 2.457

3.  Total synthesis of cribrostatin 6.

Authors:  Daniel Knueppel; Stephen F Martin
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

4.  Regio- and stereoselective monoepoxidation of dienes using methyltrioxorhenium: synthesis of allylic epoxides.

Authors:  Saroj Ranjan De; Ganesh Kumar; Jawahar L Jat; Saritha Birudaraju; Biao Lu; Rajkumar Manne; Narender Puli; Adeniyi Michael Adebesin; John R Falck
Journal:  J Org Chem       Date:  2014-10-27       Impact factor: 4.354

5.  A Domino 10-Step Total Synthesis of FR252921 and Its Analogues, Complex Macrocyclic Immunosuppressants.

Authors:  Yong Chen; Guilhem Coussanes; Caroline Souris; Paul Aillard; Dainis Kaldre; Kathrin Runggatscher; Stefan Kubicek; Giovanni Di Mauro; Boris Maryasin; Nuno Maulide
Journal:  J Am Chem Soc       Date:  2019-08-22       Impact factor: 16.383

  5 in total

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