Stereoselective Syntheses of Tetrahydropyrans Applications to the Synthesis of (+)-Leucascandrolide A, (+)-Dactylolide and (±)-Diospongin A
by
Lee, Kiyoun. author.
Başlık
:
Stereoselective Syntheses of Tetrahydropyrans Applications to the Synthesis of (+)-Leucascandrolide A, (+)-Dactylolide and (±)-Diospongin A
Yazar
:
Lee, Kiyoun. author.
ISBN
:
9783319044620
Ek Yazar
:
Lee, Kiyoun. author.
Fiziksel Tanım
:
XIX, 184 p. 256 illus., 12 illus. in color. online resource.
Series
:
Springer Theses, Recognizing Outstanding Ph.D. Research,
Contents
:
Introduction -- Significance -- General Approaches to the Synthesis of Substituted Tetrahydropyrans -- Stereoselective Synthesis of Tetrahydropyrans via Tandem and Organocatalytic Oxa-Conjugate Addition Reactions -- Introduction -- Preliminary Study -- Result and Discussion -- Synthesis of 4-Hydroxy-2,6-cis-Tetrahydropyrans via Tandem Cross-Metathesis/Thermal SN2′ Reaction.
Abstract
:
In his thesis, Kiyoun Lee describes his studies into tandem and organocatalytic oxa-conjugate addition reactions for the synthesis of complex tetrahydropyrans (THP). Readers gain insight into the new methods Lee employs for the synthesis of biologically interesting natural products including (+)-leucascandrolide A, (+)-dactylolide, and (±)-diospongin A. The reactions Lee investigates are applicable to a broad range of substrates and proceed with excellent stereoselectivity. Moreover, the methodologies allow the synthesis of a wide range of THP-containing compounds. The development of reactions, such as those discussed by Lee, has the potential to impact natural product synthesis, pharmaceutical development and chemical biology. .
Konu Terimleri
:
Chemistry.
Pharmaceutical technology.
Organic chemistry.
Chemical engineering.
Pharmaceutical Sciences/Technology.
Industrial Chemistry/Chemical Engineering.
Added Corporate Author
:
SpringerLink (Online service)
Electronic Access
:
| Library | Materyal Türü | Barkod | Yer Numarası | Durum |
|---|
| Pamukkale Merkez Kütüphanesi | E-Kitap | 75677-1001 | QD415 -436 | Springer |