Practical syntheses of the C12–C21 epothilone subunit via catalytic asymmetric reductions: Itsuno–Corey oxazaborolidine reduction and asymmetric Noyori hydrogenation-Reference-Cited by-同舟云学术

Practical syntheses of the C12–C21 epothilone subunit via catalytic asymmetric reductions: Itsuno–Corey oxazaborolidine reduction and asymmetric Noyori hydrogenation

Published:2004-07 Issue:30 Volume:45 Page:5845-5847
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Reiff Emily A,Nair Sajiv K,Narayan Reddy B.S,Inagaki Jun,Henri John T,Greiner Jack F,Georg Gunda I

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Epothilone A and B—Novel 16-Membered Macrolides with Cytotoxic Activity: Isolation, Crystal Structure, and Conformation in Solution

2. Activities of the Microtubule-stabilizing Agents Epothilones A and B with Purified Tubulin and in Cells Resistant to Paclitaxel (Taxol®)

3. The Biology and Medicinal Chemistry of Epothilones

4. Chemical Biology of Epothilones

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1. Asymmetric hydrogenation of exocyclic γ,δ-unsaturated β-ketoesters to functionalized chiral allylic alcohols via dynamic kinetic resolution;Chemical Science;2021

2. Itsuno's reagent;Catalysis from A to Z;2020-04-19

3. A Scalable Approach for the Synthesis of Epothilone Thiazole Fragment (C12–C21 unit) Via Wacker Oxidation;Synlett;2018-02-22

4. Coordination determined chemo- and enantioselectivities in asymmetric hydrogenation of multi-functionalized ketones;Coordination Chemistry Reviews;2018-01

5. Preparation of γ,δ-unsaturated-β-ketoesters: Lewis acid-catalysed C H insertion of ethyl diazoacetate into α,β-unsaturated aldehydes;Tetrahedron Letters;2017-09