Literature DB >> 27498628

Diaza [1,4] Wittig-type rearrangement of N-allylic-N-Boc-hydrazines into γ-amino-N-Boc-enamines.

Eiji Tayama1, Yoshiaki Kobayashi1, Yuka Toma1.   

Abstract

Diaza [1,4] Wittig-type rearrangement of N-allylic-N-Boc-hydrazines into γ-amino-N-Boc-enamines was demonstrated. The scope and limitation, experimental mechanistic studies, and a proposed reaction mechanism were also described.

Entities:  

Year:  2016        PMID： 27498628     DOI： 10.1039/c6cc04626f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  2 in total

1.  Synthesis and Magnetic Properties of Stable Radical Derivatives Carrying a Phenylacetylene Unit.

Authors:  Shogo Miyashiro; Tomoaki Ishii; Youhei Miura; Naoki Yoshioka
Journal:  Molecules       Date:  2018-02-09       Impact factor: 4.411

2.  Basicity-Tuned Reactivity: diaza-[1,2]-Wittig versus diaza-[1,3]-Wittig Rearrangements of 3,4-Dihydro-2H-1,2,3-benzothiadiazine 1,1-Dioxides.

Authors:  Imre Gyűjtő; Márta Porcs-Makkay; Gergő Szabó; Zsolt Kelemen; Gyöngyvér Pusztai; Gábor Tóth; András Dancsó; Judit Halász; Gyula Simig; Balázs Volk; László Nyulászi
Journal:  J Org Chem       Date:  2020-12-31       Impact factor: 4.354
  2 in total

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