z-logo
Premium
Asymmetric Total Synthesis of Cylindrocyclophanes A and F through Cyclodimerization and a Ramberg–Bäcklund Reaction
Author(s) -
Nicolaou K. C.,
Sun YaPing,
Korman Henry,
Sarlah David
Publication year - 2010
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201003500
Subject(s) - chemistry , stereochemistry
Two make a cycle : A Ramberg–Bäcklund reaction was employed to form the macrocyclic carbon skeleton of the marine natural products cylindrocyclophanes A and F in an asymmetric synthesis through a head‐to‐tail dimerization approach (see scheme).

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