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10 in total

Review 1. Antiplasmodial marine natural products in the perspective of current chemotherapy and prevention of malaria: a review.

Authors: Dominique Laurent; Francesco Pietra
Journal: Mar Biotechnol (NY) Date: 2006-03-30 Impact factor: 3.619

2. Total synthesis of the Lycopodium alkaloid serratezomine A using free radical-mediated vinyl amination to prepare a β-stannyl enamine linchpin.

Authors: Julie A Pigza; Jeong-Seok Han; Aroop Chandra; Daniel Mutnick; Maren Pink; Jeffrey N Johnston
Journal: J Org Chem Date: 2012-12-28 Impact factor: 4.354

3. Aza-[3 + 3] Annulations: A New Unified Strategy in Alkaloid Synthesis.

Authors: Grant S Buchanan; John B Feltenberger; Richard P Hsung
Journal: Curr Org Synth Date: 2010-08-01 Impact factor: 1.975

4. A Stereodivergent Approach for Accessing Both C2,8a-Syn and C2,8a-Anti Relative Stereochemical Manifolds in the Lepadin Family via a TiCL(4)-Promoted Aza-[3 + 3] Annulation.

Authors: Gang Li; Lauren J Carlson; Irina K Sagamanova; Brian W Slafer; Richard P Hsung; Claudio Gilardi; Heather M Sklenicka; Nadiya Sydroenko
Journal: Synthesis (Stuttg) Date: 2009-09-01 Impact factor: 3.157

5. Assignment of the C5' relative stereochemistry in (+)-lepadin F and (+)-lepadin G and absolute configuration of (+)-lepadin G.

Authors: Gang Li; Richard P Hsung
Journal: Org Lett Date: 2009-10-15 Impact factor: 6.005

6. Lepadins I-K, 3- O-(3'-Methylthio)acryloyloxy-decahydroquinoline Esters from a Bahamian Ascidian Didemnum sp. Assignment of Absolute Stereostructures.

Authors: Sesselja Ómarsdóttir; Xiao Wang; Hong-Bing Liu; Brendan M Duggan; Tadeusz F Molinski
Journal: J Org Chem Date: 2018-10-26 Impact factor: 4.354

10. Insights into Cytotoxic Behavior of Lepadins and Structure Elucidation of the New Alkaloid Lepadin L from the Mediterranean Ascidian Clavelina lepadiformis.

Authors: Marcello Casertano; Massimo Genovese; Paolo Paoli; Alice Santi; Anna Aiello; Marialuisa Menna; Concetta Imperatore
Journal: Mar Drugs Date: 2022-01-11 Impact factor: 5.118

10 in total

Total synthesis of lepadins B, d, e, and h; determination of the configuration of the latter three alkaloids.