Premium
5‐Bromobenzofuran Analog of Chloramphenicol
Author(s) -
Bevinakatti Hanamanthsa S.,
Badiger Virupax V.
Publication year - 1982
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570190111
Subject(s) - chemistry , fragmentation (computing) , propane , diol , chloramphenicol , medicinal chemistry , stereochemistry , organic chemistry , antibiotics , biochemistry , computer science , operating system
dl‐threo ‐2‐Dichloroacetamido‐1‐[2‐(5‐bromobenzofuranyl)] propane‐1, 3‐diol ( 7 ) was synthesised according to Sorm's method. The fragmentation of 2‐dichloroacetamido‐3‐hydroxy‐1‐[2‐(5‐bromobenzofuranyl)[‐1‐propanone ( 6 ) under electron impact is reported. The base peak is due to the rupture of the central bond whereas loss of water and McLafferty rearrangement also lead to important fragmentation pathways.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom