Inverse Amine‐Stabilized Sulfenes F 2 CSO 2  and FHCSO 2 | Zendy

Pritzkow Hans | Zendy; Rall Klaus | Zendy; ReimannAndersen Stefan | Zendy; Sundermeyer Wolfgang | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Inverse Amine‐Stabilized Sulfenes F 2 CSO 2 and FHCSO 2

Author(s) -

Pritzkow Hans,

Rall Klaus,

ReimannAndersen Stefan,

Sundermeyer Wolfgang

Publication year - 1990

Publication title -

angewandte chemie international edition in english

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 0570-0833

DOI - 10.1002/anie.199000601

Subject(s) - aminolysis , electrophile , chemistry , amine gas treating , adduct , atom (system on chip) , stereochemistry , organic chemistry , computer science , catalysis , embedded system

An electrophilic C atom distinguishes the two title sulfenes from other sulfenes, in which the S atom is electrophilic. This follows from the structures of the Et 3 N adducts. which in these cases are present as zwitterions 1 and 2 respectively, and do not have the general structure A. 2 is formed from FH 2 CSO 2 C1 and Et 3 N, 1 by aminolysis of the dithietane 3 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research