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- A stereoselective approach to indolizidine and pyrrolizidine alkaloids: total synthesis of (−)-lentiginosine, (−)-epi-lentiginosine and (−)-dihydroxypyrrolizidine. Shruti Vandana Kauloorkar, Vishwajeet Jha, Ganesh Jogdand, Pradeep Kumar
, Org. Biomol. Chem.
, 2014
, 12
, 4454
- Synthesis of pyrrolidine iminosugars, (−)-lentiginosine, (−)-swainsonine and their 8a-epimers from d-glycals. Alafia A. Ansari, Y. D. Vankar
, RSC Adv.
, 2014
, 4
, 12555
- Asymmetric syntheses of (−)-lentiginosine and an original pyrrolizidinic analogue thereof from a versatile epoxyamine intermediate. Tahar Ayad, Yves Génisson, Michel Baltas
, Org. Biomol. Chem.
, 2005
, 3
, 2626
- Practical synthesis of trans-dihydroxybutyrolactols as chiral C4 building blocks and their application to the synthesis of polyhydroxylated alkaloids. Jing Zeng, Qian Zhang, Hong-Kui Zhang, Anqi Chen
, RSC Adv.
, 2013
, 3
, 20298
- Concise asymmetric syntheses of (−)-lentiginosine and of its pyrrolizidinic analogue. Tahar Ayad, Yves Génisson, Michel Baltas, Liliane Gorrichon
, Chem. Commun.
, 2003
, 582
- Enantioselective syntheses of (R)-pipecolic acid, (2R,3R)-3-hydroxypipecolic acid, β-(+)-conhydrine and (−)-swainsonine using an aziridine derived common chiral synthon. Subhash P. Chavan, Lalit B. Khairnar, Kailash P. Pawar, Prakash N. Chavan, Sanket A. Kawale
, RSC Adv.
, 2015
, 5
, 50580
- Cyclic enaminones. Part II: applications as versatile intermediates in alkaloid synthesis. Amit Kumar Chattopadhyay, Stephen Hanessian
, Chem. Commun.
, 2015
, 51
, 16450
- Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines. F. M. Cordero, C. Vurchio, C. Faggi, A. Brandi
, Org. Chem. Front.
, 2016
, 3
, 1651
- Indolizidine and quinolizidine alkaloids. Joseph P. Michael
, Nat. Prod. Rep.
, 2003
, 20
, 458
- Synthesis of polyhydroxylated pyrrolidines from sugar-derived bromonitriles through a cascade addition of allylmagnesium bromide/cyclization/reduction. Michał Malik, Sławomir Jarosz
, Org. Biomol. Chem.
, 2016
, 14
, 1764