Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/22909
Title: Synthesis of natural products by intramolecular Michael addition
Authors: Song, Ping
Keywords: DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
Issue Date: 2009
Source: Song, P. (2009). Synthesis of natural products by intramolecular Michael addition. Doctoral thesis, Nanyang Technological University, Singapore.
Abstract: The intramolecular hetero-Michael addition is one of the most convergent strategies for the synthesis of six membered heterocyclic rings from α,β-unsaturated carbonyl compounds. However, the selection of suitable precursors for the Michael addition so as to provide the efficient stereocontrol is still a challenging issue and seldom reported in the literature. The emphasis of this thesis is placed on the investigation of efficient stereochemistry control in the synthesis of natural products such as (-)-monomorine (I), diospongin A and clavosolide A. The emphasis of this thesis is placed on the investigation of efficient stereochemistry control in the synthesis of natural products such as (-)-monomorine (I), diospongin A and clavosolide A.
URI: https://hdl.handle.net/10356/22909
DOI: 10.32657/10356/22909
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Theses

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