z-logo
Premium
Samarium Iodide Induced Intramolecular C‐Glycoside Formation: Efficient Radical Formation in the Absence of an Additive
Author(s) -
Mazéas Daniel,
Skrydstrup Troels,
Doumeix Olivier,
Beau JeanMarie
Publication year - 1994
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.199413831
Subject(s) - intramolecular force , iodide , chemistry , samarium , samarium diiodide , glycoside , stereochemistry , medicinal chemistry , organic chemistry
With pyridylsulfonyl instead of phenylsulfonyl leaving groups sugar derivatives such as 1 undergo radical cyclization promoted by SmI 2 . 5‐ exo Cyclization finally results in C‐glycosides of type 2 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom