Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and Premalbrancheamide.

Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim report. Acc Chem Res (2003) 2.28

Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells. J Am Chem Soc (2002) 2.26

Enantioselective total synthesis of avrainvillamide and the stephacidins. J Am Chem Soc (2006) 1.87

Short, enantioselective total synthesis of stephacidin A. Angew Chem Int Ed Engl (2005) 1.39

Isolation of antipodal (-)-versicolamide B and notoamides L-N from a marine-derived Aspergillus sp. Org Lett (2009) 1.35

Improved biomimetic total synthesis of D,L-stephacidin A. Org Lett (2007) 1.25

Asymmetric total syntheses of (+)- and (-)-versicolamide B and biosynthetic implications. Nat Chem (2009) 1.22

Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids. J Nat Prod (2012) 1.19

Asymmetric total synthesis of (-)-VM55599: establishment of the absolute stereochemistry and biogenetic implications. J Am Chem Soc (2002) 1.16

Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids. Chem Soc Rev (2009) 1.10

Premalbrancheamide: synthesis, isotopic labeling, biosynthetic incorporation, and detection in cultures of Malbranchea aurantiaca. Org Lett (2008) 1.04

Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide. Org Lett (2011) 1.00

Isolation and photoinduced conversion of 6-epi-stephacidins from Aspergillus taichungensis. Org Lett (2013) 0.90

Studies on the Biosynthesis of the Stephacidin and Notoamide Natural Products: A Stereochemical and Genetic Conundrum. Isr J Chem (2011) 0.86

Natural products synthesis: enabling tools to penetrate Nature's secrets of biogenesis and biomechanism. J Org Chem (2011) 0.85

Enantioselective synthesis of (+)-malbrancheamide B. J Org Chem (2013) 0.84

The cascade radical cyclisation approach to prenylated alkaloids: synthesis of stephacidin A and notoamide B. Org Biomol Chem (2013) 0.81

Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I. Chem Sci (2015) 0.81

Synthesis of the asperparaline core by a radical cascade. Org Lett (2011) 0.80

Chrysogenamide A from an endophytic fungus associated with Cistanche deserticola and its neuroprotective effect on SH-SY5Y cells. J Antibiot (Tokyo) (2008) 0.79

Efficient entry to the [2.2.2]-diazabicyclic ring system via diastereoselective domino reaction sequence. Org Lett (2012) 0.79

Rapid access to polycyclic indolines related to the stephacidin alkaloids using a radical cascade. Chem Commun (Camb) (2011) 0.78

Adaptation of a small-molecule hydrogen-bond donor catalyst to an enantioselective hetero-Diels-Alder reaction hypothesized for brevianamide biosynthesis. Org Lett (2015) 0.77

Synthesis of Bridged Diketopiperazines by Using the Persistent Radical Effect and a Formal Synthesis of Bicyclomycin. Angew Chem Int Ed Engl (2015) 0.77

Synthesis of Peramine, an Anti-insect Defensive Alkaloid Produced by Endophytic Fungi of Cool Season Grasses. J Nat Prod (2016) 0.75

Further Investigation of the Intermolecular Diels-Alder Cycloaddition for the Synthesis of Bicyclo[2.2.2]diazaoctane Alkaloids. J Org Chem (2017) 0.75