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Application of the aza-Diels–Alder reaction in the synthesis of natural products . Min-Hui Cao, Nicholas J. Green, Sheng-Zhen Xu
, Org. Biomol. Chem.
, 2017
, 15
, 3105
A biomimetic approach for bicyclic alkaloids using acetal pro-nucleophile: total synthesis of (±)-epilupinine and formal syntheses of (±)-laburnine, (±)-isoretronecanol, (±)-tashiromine . Dipankar Koley, Kyatham Srinivas, Yarkali Krishna, Archita Gupta
, RSC Adv.
, 2014
, 4
, 3934
Indolizidine and quinolizidine alkaloids . J. P. Michael
, Nat. Prod. Rep.
, 1990
, 7
, 485
An efficient asymmetric synthesis of (−)-lupinine . Stephen G. Davies, Ai M. Fletcher, Emma M. Foster, Ian T. T. Houlsby, Paul M. Roberts, Thomas M. Schofield, James E. Thomson
, Chem. Commun.
, 2014
, 50
, 8309
Recent advances in the intramolecular Mannich reaction in natural products total synthesis . Yingbo Shi, Qiaoling Wang, Shuanhu Gao
, Org. Chem. Front.
, 2018
, 5
, 1049
The asymmetric syntheses of pyrrolizidines, indolizidines and quinolizidines via two sequential tandem ring-closure/N-debenzylation processes . Stephen G. Davies, Ai M. Fletcher, Emma M. Foster, Ian T. T. Houlsby, Paul M. Roberts, Thomas M. Schofield, James E. Thomson
, Org. Biomol. Chem.
, 2014
, 12
, 9223
Complementary enantioselective approaches to the quinolizidine alkaloids lupinine and epilupinine by enolate Claisen rearrangements or direct allylation of piperidin-2-ylacetic acid derivatives . Christopher Morley, David W. Knight, Andrew C. Share
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 2903
Reduction of sugar derivatives to valuable chemicals: utilization of asymmetric carbons . Masazumi Tamura, Yoshinao Nakagawa, Keiichi Tomishige
, Catal. Sci. Technol.
, 2020
, 10
, 3805
Asymmetric total synthesis of (+)-swainsonine . Soontorn Chooprayoon, Chutima Kuhakarn, Patoomratana Tuchinda, Vichai Reutrakul, Manat Pohmakotr
, Org. Biomol. Chem.
, 2011
, 9
, 531
Biosynthesis of quinolizidine alkaloids in lupins: mechanistic considerations and prospects for pathway elucidation . Davide Mancinotti, Karen Michiko Frick, Fernando Geu-Flores
, Nat. Prod. Rep.
, 2022
, 39
, 1423