Asymmetric organocatalytic Michael–hemiacetalization reaction: access to chiral spiro cis-δ-lactones by in situ oxidation of spiro δ-lactols-Reference-Cited by-同舟云学术

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Asymmetric organocatalytic Michael–hemiacetalization reaction: access to chiral spiro cis-δ-lactones by in situ oxidation of spiro δ-lactols

Published:2013-05 Issue:20 Volume:54 Page:2546-2548
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wei Mo-Hui,Zhou Yi-Rong,Gu Liang-Hu,Luo Fan,Zhang Fang-Lin

Funder

National Natural Science Foundation of China

The Central Colleges and Universities Basic Scientific Research Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Conception and pharmacodynamic profile of drospirenone

2. Complement-Inhibiting Iridoids from Morinda morindoides

3. Abyssomicin C—A Polycyclic Antibiotic from a MarineVerrucosispora Strain as an Inhibitor of thep-Aminobenzoic Acid/Tetrahydrofolate Biosynthesis Pathway

4. Abyssomicins, Inhibitors of the para-Aminobenzoic Acid Pathway Produced by the Marine Verrucosispora Strain AB-18-032

5. Toward the Total Synthesis of Variecolin

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