A Concise/catalytic approach for the construction of the C14–C28 fragment of eribulin
S Senapati, CV Ramana - Organic & Biomolecular Chemistry, 2021 - pubs.rsc.org
A simple approach for the synthesis of the C14–C28 fragment of eribulin has been
developed by employing a one-pot gold-catalyzed alkynol cyclization/Kishi reduction to …
developed by employing a one-pot gold-catalyzed alkynol cyclization/Kishi reduction to …
A Convergent Approach for the Synthesis of C14–C26 Fragment of Anticancer Drug Eribulin Mesylate
R Nasam, S Pabbaraja - Synthesis, 2024 - thieme-connect.com
The stereoselective synthesis of C14–C26 fragment of eribulin is reported in a convergent
way by coupling of fragment C14–C19 with fragment C20–C26 that are accessible from …
way by coupling of fragment C14–C19 with fragment C20–C26 that are accessible from …
Synthesis of the C1–C13 fragment of eribulin mesylate
H Lee, Y Park, H Jung, ST Kim, S Sin, E Ko, IS Myeong… - Tetrahedron, 2019 - Elsevier
Synthesis of the C1–C13 fragment of eribulin mesylate has been accomplished. It features a
highly stereoselective construction of a trans-dihydropyran framework using three key …
highly stereoselective construction of a trans-dihydropyran framework using three key …
Oxidations with Iodine (V) Compounds–From Stoichiometric Compounds to Catalysts
F Ballaschk, SF Kirsch - Iodine Catalysis in Organic Synthesis, 2022 - Wiley Online Library
The use of iodine (V) compounds for oxidative processes has increased dramatically in
recent decades. Their first appearance was in the early 1890s with the discovery of …
recent decades. Their first appearance was in the early 1890s with the discovery of …