Exploitation of highly functionalised epoxides derived from asymmetrized tris(hydroxymethyl)methane (THYM∗) in the synthesis of a fragment of lasalocide A and other related polyether ionofore antibiotics-Reference-Cited by-同舟云学术

Exploitation of highly functionalised epoxides derived from asymmetrized tris(hydroxymethyl)methane (THYM∗) in the synthesis of a fragment of lasalocide A and other related polyether ionofore antibiotics

Published:1996-09 Issue:38 Volume:52 Page:12631-12642
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Guanti Giuseppe,Narisano Enrica

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Asymmetrized trils (hydroxymethyl)methane as a highly stereodivergent chiral building block: preparation of all four stereoisomers of protected 2-hydroxymethyl-1,3-butanediol

2. Stereodivergent Synthesis of cis epoxides derived from asymmetrized 2-alkenyl-1,3-propanediols

3. Chemoenzymic preparation of asymmetrized tris(hydroxymethyl)methane (THYM*) and of asymmetrized bis(hydroxymethyl)acetaldehyde (BHYMA*) as new highly versatile chiral building blocks

4. Regiocontrol in reductive ring opening of epoxides derived from asymmetrized 2-alkenyl-1,3-propanediols

5. Regiocontrol in nucleophilic ring opening of chiral epoxides of chemoenzymatic origin

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2. Lithium Divinylcuprate;Encyclopedia of Reagents for Organic Synthesis;2007-09-17

3. Strategy and Methodology Development for the Total Synthesis of Polyether Ionophore Antibiotics;Chemical Reviews;2000-06-01

4. Chemoenzymatic synthesis of 2-substituted 2-fluoro-1,3-dioxygenated chiral building blocks;Tetrahedron: Asymmetry;1999-04

5. Asymmetrized Tris(hydroxymethyl)methane and Related Synthons: Enantioselective Preparation and Synthetic Applications;European Journal of Organic Chemistry;1998-05