870646-63-2Relevant academic research and scientific papers
Control of diastereoselectivity in C=O/C=N reductive cyclizations using an intramolecularly tethered hydrazone
Chiara, Jose Luis,García, ángela
, p. 2607 - 2610 (2005)
Cyclic hydrazones are efficient ketyl radical acceptors in reductive coupling cyclizations mediated by samarium diiodide, affording cyclic amino alcohols with controlled stereochemistry at the new aminated stereocenter. This approach has been successfully
