Literature DB >> 23131013

1,4-Diamination of cyclic dienes via a (4 + 3) cycloaddition of diaza-allyl cationic intermediates.

Christopher S Jeffrey1, Devendar Anumandla, Christopher R Carson.   

Abstract

Diaza-(4 + 3) cycloadditions of putative diaza-oxyallyl cationic intermediates and cyclic dienes are reported as a method for the 1,4-diamination of cyclic dienes. This reaction was entirely selective for diamination and provided cycloadducts in good to excellent yield.

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Year:  2012        PMID： 23131013     DOI： 10.1021/ol302771z

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Generation and Reactivity of 2-Amido-1,3-diaminoallyl Cations: Cyclic Guanidine Annulations via Net (3 + 2) and (4 + 3) Cycloadditions.

Authors:  V Raghavendra Rao Kovvuri; Haoran Xue; Daniel Romo
Journal:  Org Lett       Date:  2020-02-03       Impact factor: 6.005

2.  Regioselective and Diastereoselective Aminoarylation of 1,3-Dienes.

Authors:  Hongli Bao; Liela Bayeh; Uttam K Tambar
Journal:  Chem Sci       Date:  2014-12-01       Impact factor: 9.825

3.  Dearomative Indole (3 + 2) Reactions with Azaoxyallyl Cations--New Method for the Synthesis of Pyrroloindolines.

Authors:  Maria C DiPoto; Russell P Hughes; Jimmy Wu
Journal:  J Am Chem Soc       Date:  2015-11-17       Impact factor: 15.419
  3 in total

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