Jackson, Katrina L.; Henderson, James A.; Motoyoshi, Hajime, Angewandte Chemie - International Edition, 2009, vol. 48, p. 2346 - 2350
作者:Jackson, Katrina L.、Henderson, James A.、Motoyoshi, Hajime、Phillips, Andrew J.
DOI:——
日期:——
A synthesis of the C1–C15 domain of the halichondrins
作者:Katrina L. Jackson、James A. Henderson、Jonathan C. Morris、Hajime Motoyoshi、Andrew J. Phillips
DOI:10.1016/j.tetlet.2008.03.018
日期:2008.4
A concise route to the C1-C15 domain of the halichondrins is described. The key reaction is the conversion of a furfuryl alcohol to a pyranone. The stereocenter of this pyranone serves as the starting point for the other eight stereocenters. (c) 2008 Elsevier Ltd. All rights reserved.
PYRAN FUSED RING COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF
申请人:Beijing Tienyi Lufu Pharmatech Co. Ltd.
公开号:EP3608323B1
公开(公告)日:2021-11-03
[EN] PROCESS FOR PREPARATION OF ERIBULIN AND INTERMEDIATES THEREOF<br/>[FR] PROCÉDÉ DE PRÉPARATION D'ÉRIBULINE ET DE SES INTERMÉDIAIRES
申请人:DR REDDY’S LABORATORIES LTD
公开号:WO2017168309A1
公开(公告)日:2017-10-05
The present application relate to process for preparation of octahydropyrano [3, 2-b] pyran compound of formula II, which is useful as an intermediate for the preparation of halichondrin B analogues such as Eribulin or its pharmaceutically acceptable salts.