TOTAL SYNTHESIS OF THE CRINANE-TYPE AMARYLLIDACEAE ALKALOIDS (+)-MARITIDINE AND (+)-OXOMARITIDINE
The crinane-type alkaloids are characterized by the presence of the 5,10b-ethanophenanthridine skeleton and represent an important subgroup within the large family of Amaryllidaceae alkaloids, many of which exhibit interesting biological activities. Although they have been the subjects of extensive...
Main Author: | Ding, Lixin |
---|---|
Other Authors: | David E Minter |
Format: | Others |
Language: | en |
Published: |
Texas Christian University
2010
|
Subjects: | |
Online Access: | http://etd.tcu.edu/etdfiles/available/etd-04262010-120745/ |
Similar Items
-
The Theoretical Total Synthesis of an Aromatic Esters of the Crinane Amaryllidaceae Alkaloid Ambelline
by: Liu Danyang, et al.
Published: (2021-01-01) -
Derivatives of the β-Crinane Amaryllidaceae Alkaloid Haemanthamine as Multi-Target Directed Ligands for Alzheimer’s Disease
by: Eliška Kohelová, et al.
Published: (2019-04-01) -
Towards the asymmetric synthesis of (+)-maritidine
by: Sheppard, Gareth Cenydd
Published: (2016) -
SYNTHETIC APPROACHES TO THE SKELETON OF CRININE-TYPE ALKALOIDS FROM ISOQUINOLINE AND THE TOTAL SYNTHESIS OF (±)-CRININE
by: Bian, Zhiguo
Published: (2010) -
Transformations of Isocarbostyrils for the Synthesis of Isoquinoline Alkaloids and the Related Analogues
by: Huang, Yijun
Published: (2008)