Diverse Modes of Reactivity of 6‐(Chloromethyl)‐6‐methylfulvene | Zendy

Erden Ihsan | Zendy; Gronert Scott | Zendy; Cabrera Gabriel | Zendy; Coskun Necdet | Zendy; Tapken Marco | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Diverse Modes of Reactivity of 6‐(Chloromethyl)‐6‐methylfulvene

Author(s) -

Erden Ihsan,

Gronert Scott,

Cabrera Gabriel,

Coskun Necdet,

Tapken Marco

Publication year - 2017

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201700442

Subject(s) - nucleophile , chemistry , electrophile , reactivity (psychology) , enamine , stereochemistry , organic chemistry , catalysis , medicine , alternative medicine , pathology

The title compound exhibits a number of modes of reactivity toward nucleophiles/bases owing to the presence of several electrophilic and potentially nucleophilic sites in the molecule. We explored the reactions of 6‐(chloromethyl)‐6‐methylfulvene with oxygen and nitrogen nucleophiles and bases as well as a carbon‐based nucleophile (an enamine) and realized all possible reactivity modes predicted on the basis of electrophilic and nucleophilic positions in this compound.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research