Literature DB >> 15065270

8-Oxabicyclo[3.2.1]oct-6-en-3-ones: application to the asymmetric synthesis of polyoxygenated building blocks.

Ingo V Hartung1, H Martin R Hoffmann.   

Abstract

The development and design of reliable and efficient methods for the construction of chiral building blocks are crucial in modern natural product synthesis. 8-Oxabicyclo[3.2.1]oct-6-en-3-ones are readily accessible scaffolds with defined stereochemical features which have been exploited for non-aldol approaches to the preparation of chiral building blocks. Strategies for their enantioselective synthesis, including asymmetric cycloaddition methods, desymmetrization protocols, and "racemic switch operations", are presented and evaluated.

Entities:  

Year:  2004        PMID: 15065270     DOI: 10.1002/anie.200300622

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


  16 in total

1.  Total synthesis of the originally assigned structure of vannusal B.

Authors:  K C Nicolaou; Hongjun Zhang; Adrian Ortiz; Philippe Dagneau
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

2.  Regioselectivities of (4 + 3) cycloadditions between furans and oxazolidinone-substituted oxyallyls.

Authors:  Andrew G Lohse; Elizabeth H Krenske; Jennifer E Antoline; K N Houk; Richard P Hsung
Journal:  Org Lett       Date:  2010-11-04       Impact factor: 6.005

3.  Intramolecular oxyallyl-carbonyl (3 + 2) cycloadditions.

Authors:  Elizabeth H Krenske; Shuzhong He; Jian Huang; Yunfei Du; K N Houk; Richard P Hsung
Journal:  J Am Chem Soc       Date:  2013-04-01       Impact factor: 15.419

4.  Total synthesis and structural revision of vannusals A and B: synthesis of the originally assigned structure of vannusal B.

Authors:  K C Nicolaou; Adrian Ortiz; Hongjun Zhang; Philippe Dagneau; Andreas Lanver; Michael P Jennings; Stellios Arseniyadis; Raffaella Faraoni; Dimitrios E Lizos
Journal:  J Am Chem Soc       Date:  2010-05-26       Impact factor: 15.419

5.  Stereoselectivity in Oxyallyl-Furan 4+3 Cycloadditions: Control of Intermediate Conformations and Dispersive Stabilisation with Evans' Oxazolidinones.

Authors:  Elizabeth H Krenske; K N Houk; Andrew G Lohse; Jennifer E Antoline; Richard P Hsung
Journal:  Chem Sci       Date:  2010-09-01       Impact factor: 9.825

6.  Developing a diastereoselective intramolecular [4+3] cycloaddition of nitrogen-stabilized oxyallyl cations derived from N-sulfonyl-substituted allenamides.

Authors:  Andrew G Lohse; Richard P Hsung; Mitchell D Leider; Sunil K Ghosh
Journal:  J Org Chem       Date:  2011-04-08       Impact factor: 4.354

7.  Stereocontrolled Syntheses of Seven-Membered Carbocycles by Tandem Allene Aziridination/[4+3] Reaction.

Authors:  Nels C Gerstner; Christopher S Adams; Maik Tretbar; Jennifer M Schomaker
Journal:  Angew Chem Int Ed Engl       Date:  2016-10-10       Impact factor: 15.336

8.  Stereoselectivities and regioselectivities of (4 + 3) cycloadditions between allenamide-derived chiral oxazolidinone-stabilized oxyallyls and furans: experiment and theory.

Authors:  Jennifer E Antoline; Elizabeth H Krenske; Andrew G Lohse; K N Houk; Richard P Hsung
Journal:  J Am Chem Soc       Date:  2011-08-18       Impact factor: 15.419

9.  Control of regioselectivity and stereoselectivity in (4 + 3) cycloadditions of chiral oxyallyls with unsymmetrically disubstituted furans.

Authors:  Yunfei Du; Elizabeth H Krenske; Jennifer E Antoline; Andrew G Lohse; K N Houk; Richard P Hsung
Journal:  J Org Chem       Date:  2012-07-31       Impact factor: 4.354

10.  Gold-catalyzed transannular [4+3] cycloaddition reactions.

Authors:  Benjamin W Gung; Derek T Craft; Lauren N Bailey; Kristin Kirschbaum
Journal:  Chemistry       Date:  2010-01-11       Impact factor: 5.236

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