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Literature DB >> 28748936

Organic chemistry: Molecular structure assignment simplified.

Severin K Thompson¹, Thomas R Hoye¹.

Abstract

Mesh：

Year: 2017 PMID： 28748936 DOI： 10.1038/547410a

Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962

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7 in total

Review 1. Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation.

Authors: K C Nicolaou; Scott A Snyder
Journal: Angew Chem Int Ed Engl Date: 2005-02-04 Impact factor: 15.336

2. Total Synthesis of Reported Structure of Baulamycin A and Its Congeners.

Authors: Sandip Guchhait; Shamba Chatterjee; Ravi Sankar Ampapathi; Rajib Kumar Goswami
Journal: J Org Chem Date: 2017-02-23 Impact factor: 4.354

3. Fluorous mixture synthesis: a fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds.

Authors: Z Luo; Q Zhang; Y Oderaotoshi; D P Curran
Journal: Science Date: 2001-03-02 Impact factor: 47.728

4. Baulamycins A and B, broad-spectrum antibiotics identified as inhibitors of siderophore biosynthesis in Staphylococcus aureus and Bacillus anthracis.

Authors: Ashootosh Tripathi; Michael M Schofield; George E Chlipala; Pamela J Schultz; Isaiah Yim; Sean A Newmister; Tyler D Nusca; Jamie B Scaglione; Philip C Hanna; Giselle Tamayo-Castillo; David H Sherman
Journal: J Am Chem Soc Date: 2014-01-17 Impact factor: 15.419

Organic chemistry: Molecular structure assignment simplified.

Review 1. Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation.

2. Total Synthesis of Reported Structure of Baulamycin A and Its Congeners.

3. Fluorous mixture synthesis: a fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds.

4. Baulamycins A and B, broad-spectrum antibiotics identified as inhibitors of siderophore biosynthesis in Staphylococcus aureus and Bacillus anthracis.

5. Synergy of synthesis, computation and NMR reveals correct baulamycin structures.

6. Accuracy in determining interproton distances using Nuclear Overhauser Effect data from a flexible molecule.

7. Assembly-line synthesis of organic molecules with tailored shapes.