Literature DB >> 11456477

Exploration of fundamental and synthetic aspects of the intramolecular 4 + 3 cycloaddition reaction.

M Harmata1.   

Abstract

In this Account, a summary of our work in the exploration and development of intramolecular 4 + 3 cycloaddition reactions between dienes and allylic cations is presented. Alkoxyallylic sulfones are useful precursors for the generation of allylic cations which are good dienophiles. Such substrates allowed a number of important pieces of data concerning the cycloaddition to be obtained. The evolution of the work has involved pursuing other methods for allylic cation generation, an investigation of stereochemical variables and applications, including the total syntheses of aphanamol I, widdrol, and (+)-dactylol.

Entities:  

Year:  2001        PMID: 11456477     DOI: 10.1021/ar000064e

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  13 in total

1.  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

2.  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

3.  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

4.  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

5.  Tandem processes identified from reaction screening: nucleophilic addition to aryl N-phosphinylimines employing La(III)-TFAA activation.

Authors:  Hidenori Kinoshita; Oscar J Ingham; Winnie W Ong; Aaron B Beeler; John A Porco
Journal:  J Am Chem Soc       Date:  2010-05-12       Impact factor: 15.419

6.  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

7.  (3+2)-Cycloaddition Reactions of Oxyallyl Cations.

Authors:  Hui Li; Jimmy Wu
Journal:  Synthesis (Stuttg)       Date:  2015-01       Impact factor: 3.157

8.  Mechanistic Perspectives in the Regioselective Indole Addition to Unsymmetrical Silyloxyallyl Cations.

Authors:  Caitlin G Bresnahan; Kiara A Taylor-Edinbyrd; Alexander H Cleveland; Joshua A Malone; Nitin S Dange; Anne Milet; Revati Kumar; Rendy Kartika
Journal:  J Org Chem       Date:  2019-05-16       Impact factor: 4.354

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.  The first transannular [4+3] cycloaddition reaction: synthesis of the ABCD ring structure of cortistatins.

Authors:  Derek T Craft; Benjamin W Gung
Journal:  Tetrahedron Lett       Date:  2008-10-06       Impact factor: 2.415

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