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paraherquamide (87) 87
chemistry, organic (54) 54
biosynthesis (50) 50
antiparasitic agents (37) 37
index medicus (33) 33
molecular structure (32) 32
penicillium-charlesii (25) 25
chemistry, multidisciplinary (23) 23
animals (22) 22
biomimetic total-synthesis (20) 20
alkaloids (19) 19
indole alkaloids - chemistry (19) 19
stereoisomerism (19) 19
article (18) 18
chemistry, medicinal (16) 16
paraherquamides (16) 16
stephacidin-a (16) 16
anthelmintic activity (15) 15
construction (15) 15
stereocontrolled total-synthesis (15) 15
metabolites (14) 14
indole alkaloids - chemical synthesis (13) 13
marcfortine (13) 13
pharmacology & pharmacy (13) 13
brevianamides (12) 12
chemical properties (12) 12
indoles (12) 12
x-ray-analysis (12) 12
asperparaline (11) 11
cyclization (11) 11
enantioselective total-synthesis (11) 11
research (11) 11
anthelmintics - pharmacology (10) 10
aspergillus - chemistry (10) 10
brevianamide-a (10) 10
indoles - chemistry (10) 10
marine-derived fungus (10) 10
spiro compounds - chemical synthesis (10) 10
spiro compounds - chemistry (10) 10
analysis (9) 9
diels-alder reaction (9) 9
penicillium-brevicompactum (9) 9
alkaloids - chemistry (8) 8
aspergillus - metabolism (8) 8
diels-alder cycloaddition (8) 8
indole alkaloids (8) 8
indoles - chemical synthesis (8) 8
natural products (8) 8
prenylated indole alkaloids (8) 8
solid cultures (8) 8
spiro compounds - pharmacology (8) 8
structure (8) 8
vm55599 ring-systems (8) 8
aspergillus-japonicus jv-23 (7) 7
asymmetric synthesis (7) 7
avrainvillamide (7) 7
brevianamide (7) 7
diels-alder cyclizations (7) 7
indole alkaloids - metabolism (7) 7
plant sciences (7) 7
trichostrongylus-colubriformis (7) 7
aspergillus (6) 6
asymmetric-synthesis (6) 6
biochemistry & molecular biology (6) 6
brevianamide-b (6) 6
catalysis (6) 6
indole (6) 6
indolizines - chemical synthesis (6) 6
indolizines - pharmacology (6) 6
malbrancheamide (6) 6
nuclear magnetic resonance, biomolecular (6) 6
prenylation (6) 6
ring formation (6) 6
anthelmintics - chemical synthesis (5) 5
chemical modification (5) 5
chemistry, applied (5) 5
concise (5) 5
cycloaddition (5) 5
haemonchus - drug effects (5) 5
humans (5) 5
indole alkaloids - isolation & purification (5) 5
indolizines - chemistry (5) 5
meriones-unguiculatus (5) 5
models, molecular (5) 5
parasitology (5) 5
piperazines (5) 5
sheep (5) 5
stereocontrolled total synthesis (5) 5
amides - chemistry (4) 4
analogs (4) 4
anthelmintics - therapeutic use (4) 4
antineoplastic agents - chemistry (4) 4
aspergillus sp (4) 4
aspergillus-fumigatus (4) 4
chemistry (4) 4
concise synthesis (4) 4
crystallography, x-ray (4) 4
derivatives (4) 4
efficacy (4) 4
fermentation (4) 4
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1. Full Text Asperversiamides, Linearly Fused Prenylated Indole Alkaloids from the Marine-Derived Fungus Aspergillus versicolor
by Li, Huaqiang and Sun, Weiguang and Deng, Mengyi and Zhou, Qun and Wang, Jianping and Liu, Junjun and Chen, Chunmei and Qi, Changxing and Luo, Zengwei and Xue, Yongbo and Zhu, Hucheng and Zhang, Yonghui
The Journal of Organic Chemistry, ISSN 0022-3263, 08/2018, Volume 83, Issue 15, pp. 8483 - 8492
Asperversiamides A–H (1–8), eight linearly fused prenylated indole alkaloids featuring an unusual pyrano­[3,2-f]­indole unit, were isolated from the... 
CHEMISTRY, ORGANIC | RING-SYSTEM | BIOSYNTHESIS | PARAHERQUAMIDE
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2. Full Text Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, Aspergillus sp
by Kato, Hikaru and Yoshida, Takushi and Tokue, Takanori and Nojiri, Yuka and Hirota, Hiroshi and Ohta, Tomihisa and Williams, Robert M and Tsukamoto, Sachiko
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2007, Volume 46, Issue 13, pp. 2254 - 2256
Mussel power: The structures and configurations have been determined of four new indole alkaloids, notoamides A–D, which were isolated from mussel‐derived... 
natural products | indoles | structure elucidation | NMR spectroscopy | metabolites | Indoles | Metabolites | Natural products | Structure elucidation | ACID | SPONGE | PARAHERQUAMIDE | INHIBITORS | CHEMISTRY, MULTIDISCIPLINARY
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3. Full Text Comment on "Asymmetric syntheses of sceptrin andmassadine and evidence for biosynthetic enantiodivergence"
by Sherman, DH and Tsukamoto, S and Williams, RM
SCIENCE, ISSN 0036-8075, 07/2015, Volume 349, Issue 6244
Ma et al. (Reports, 10 October 2014, p. 219) report asymmetric syntheses of sceptrin and massadine and, through a stereochemical reassignment, claim to... 
EVOLUTION | METABOLISM | MULTIDISCIPLINARY SCIENCES | SYNTHASES | PARAHERQUAMIDE | FUNCTIONAL-CHARACTERIZATION
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4. Full Text Paraherquamide J, a new prenylated indole alkaloid from the marine-derived fungus Penicillium janthinellum HK1-6
by Zheng, Yao-Yao and Shen, Nan-Xing and Liang, Zhao-Yang and Shen, Li and Chen, Min and Wang, Chang-Yun
Natural Product Research, ISSN 1478-6419, 2019, pp. 1 - 7
A new prenylated indole alkaloid, named paraherquamide J (1), together with four known compounds (2-5), were isolated from the mangrove rhizosphere... 
prenylated indole alkaloid | paraherquamide | marine-derived fungus; Penicillium janthinellum
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5. Full Text Angularly Prenylated Indole Alkaloids with Antimicrobial and Insecticidal Activities from an Endophytic Fungus Fusarium sambucinum TE-6L
by Zhang, P and Yuan, XL and Du, YM and Zhang, HB and Shen, GM and Zhang, ZF and Liang, YJ and Zhao, DL and Xu, K
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, ISSN 0021-8561, 10/2019, Volume 67, Issue 43, pp. 11994 - 12001
Bioactivity-guided isolation of the endophytic fungus Fusarium sambucinum TE-6L residing in Nicotiana tabacum L. led to the discovery of two new angularly... 
biopesticide | antimicrobial | METABOLITES | prenylated indole alkaloids | BIOSYNTHESIS | FOOD SCIENCE & TECHNOLOGY | PARAHERQUAMIDE | AGRICULTURE, MULTIDISCIPLINARY | Fusarium sambucinum | CHEMISTRY, APPLIED | MARINE | insecticidal | Index Medicus
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6. Full Text Taichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404)
by Kagiyama, Ippei and Kato, Hikaru and Nehira, Tatsuo and Frisvad, Jens C and Sherman, David H and Williams, Robert M and Tsukamoto, Sachiko
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2016, Volume 55, Issue 3, pp. 1128 - 1132
Seven new prenylated indole alkaloids, taichunamides A–G, were isolated from the fungus Aspergillus taichungensis (IBT 19404). Taichunamides A and B contained... 
natural products | cycloaddition | structure elucidation | alkaloids | biosynthesis | USTUS | PARAHERQUAMIDE | PENICILLIUM-SIMPLICISSIMUM AK-40 | MARINE-DERIVED FUNGUS | MALBRANCHEAMIDE | CHEMISTRY, MULTIDISCIPLINARY | Alkaloids | Diels-Alder reaction | Cores | Fungi | Indole | Congeners
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7. Full Text Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)‐Stephacidin A and (+)‐Notoamide B from Aspergillus versicolor NRRL 35600
by Greshock, Thomas J and Grubbs, Alan W and Jiao, Ping and Wicklow, Donald T and Gloer, James B and Williams, Robert M
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2008, Volume 47, Issue 19, pp. 3573 - 3577
Stereochemically unique: A new prenylated indole alkaloid, (+)‐versicolamide B, has been isolated from cultures of Aspergillus versicolor NRRL 35600. The... 
natural products | indoles | structure elucidation | biomimetic synthesis | Diels–Alder reaction | Diels-Alder reaction | Indoles | Natural products | Structure elucidation | Biomimetic synthesis | PARAHERQUAMIDE | MARINE-DERIVED FUNGUS | RING-SYSTEM | CHEMISTRY, MULTIDISCIPLINARY | DIELS-ALDER CYCLOADDITION | FUNGICOLOUS ISOLATE | STEPHACIDIN-A | AVRAINVILLAMIDE | BIOSYNTHESIS | ENANTIOSELECTIVE TOTAL-SYNTHESIS | CONCISE SYNTHESIS | Biomimetics - methods | Indole Alkaloids - chemical synthesis | Indole Alkaloids - isolation & purification | Indole Alkaloids - chemistry | Aspergillus - chemistry | Biosynthetic Diels-Alder | ent-notoamide B | sclerotiamide | ent-stephacidin A
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8. Full Text Rapid Access to Spirocyclic Oxindole Alkaloids: Application of the Asymmetric Palladium-Catalyzed [3 + 2] Trimethylenemethane Cycloaddition
by Trost, Barry M and Bringley, Dustin A and Zhang, Ting and Cramer, Nicolai
Journal of the American Chemical Society, ISSN 0002-7863, 11/2013, Volume 135, Issue 44, pp. 16720 - 16735
The marcfortines are complex secondary metabolites that show potent anthelmintic activity and are characterized by the presence of a bicyclo[2.2.2]diazaoctane... 
PENICILLIUM-CHARLESII | BIOMIMETIC TOTAL-SYNTHESIS | PARAHERQUAMIDE CLASS | BIOSYNTHESIS | STEREOCONTROLLED TOTAL-SYNTHESIS | X-RAY-ANALYSIS | ANTIPARASITIC AGENTS | DIELS-ALDER CYCLIZATIONS | ENANTIOSELECTIVE CONSTRUCTION | CHEMISTRY, MULTIDISCIPLINARY | STEPHACIDIN-A | Oxindoles | Methane - analogs & derivatives | Heterocyclic Compounds, 4 or More Rings - chemistry | Indoles - chemical synthesis | Models, Molecular | Alkaloids - chemical synthesis | Crystallography, X-Ray | Heterocyclic Compounds, 4 or More Rings - chemical synthesis | Indolizines - chemical synthesis | Cyclization | Indole Alkaloids - chemical synthesis | Indolizines - chemistry | Spiro Compounds - chemical synthesis | Methane - chemistry | Molecular Structure | Catalysis | Indole Alkaloids - chemistry | Indoles - chemistry | Palladium - chemistry | Alkaloids - chemistry | Spiro Compounds - chemistry | Alkaloids | Usage | Palladium | Research | Ring formation (Chemistry)
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9. Full Text Tertiary-Amine-Catalyzed Asymmetric [3+2] Annulations of Morita–Baylis–Hillman Carbonates of Isatins with Nitroolefins to Construct Spirooxindoles
by Peng, Jing and Ran, Guang-Yao and Du, Wei and Chen, Ying-Chun
Synthesis, ISSN 0039-7881, 09/2015, Volume 47, Issue 17, pp. 2538 - 2544
Abstract An enantioselective [3+2] annulation of nitroolefins with racemic Morita–Baylis–Hillman carbonates of isatins catalyzed by α-isocupreine has been... 
special topic | spirooxindole | cyclopentadiene | asymmetric [3+2] annulation | Morita-Baylis-Hillman carbonates | ENANTIOSELECTIVE SYNTHESIS | CITRINADIN-A | NATURAL-PRODUCTS | PARAHERQUAMIDE | OXINDOLES | CHEMISTRY, ORGANIC | MARINE-DERIVED FUNGUS | QUATERNARY CENTERS | PENICILLIUM-CHARLESII | CYCLOADDITION | ANTIPARASITIC AGENTS
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10. Full Text Chemo- and Diastereoselective Synthesis of N-Propargyl Oxazolidines through a Copper-Catalyzed Domino A(3) Reaction
by Zhang, YZ and Huang, LL and Li, XY and Wang, L and Feng, HD
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 05/2019, Volume 84, Issue 9, pp. 5046 - 5055
Herein we describe a highly chemoselective A(3)-coupling/annulation of amino alcohols, formaldehyde, two kinds of aldehydes and alkynes, catalyzed by... 
ASYMMETRIC-SYNTHESIS | ENANTIOSELECTIVE SYNTHESIS | FORMAL SYNTHESIS | 1,3-OXAZOLIDINES | PARAHERQUAMIDES | BIOSYNTHESIS | CHEMISTRY, ORGANIC | STEREOSELECTIVE-SYNTHESIS | YLIDES | DOCETAXEL ANALOGS | 1,3,5-TRIOXAZATRIQUINANE SKELETON
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11. Full Text New prenylated indole alkaloids from fungus Penicillium sp. derived of mangrove soil sample
by Yang, Bin and Dong, Junde and Lin, Xiuping and Zhou, Xuefeng and Zhang, Yanying and Liu, Yonghong
Tetrahedron, ISSN 0040-4020, 06/2014, Volume 70, Issue 25, pp. 3859 - 3863
Three diprenylated indole alkaloids, mangrovamides A–C ( – ), featured a bicyclo [2.2.2] diazaoctane core and possessed a novel γ-methyl proline and isoprene... 
Penicillium sp | X-ray diffraction | Prenylated indole alkaloids | Mangrovamides | Anti-acetylcholinesterase activity | CELLS | ASPERGILLUS-JAPONICUS | BIOSYNTHESIS | PARAHERQUAMIDE | MARCFORTINE | CHEMISTRY, ORGANIC | MALBRANCHEAMIDE | Fungi | Alkaloids | Dimethyl | Penicillium | X-rays | Indoles | Soil (material) | Isoprene
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12. Full Text Asymmetric total syntheses of (+)- and (−)-versicolamide B and biosynthetic implications
by Miller, Kenneth A and Tsukamoto, Sachiko and Williams, Robert M
Nature Chemistry, ISSN 1755-4330, 04/2009, Volume 1, Issue 1, pp. 63 - 68
The Diels-Alder reaction is one of the most well-studied, synthetically useful organic transformations. Although it has been postulated that a significant... 
BIOMIMETIC TOTAL-SYNTHESIS | PARAHERQUAMIDE | CONSTRUCTION | BREVIANAMIDE | CONCISE SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | DIELS-ALDER CYCLOADDITION | VM55599 RING-SYSTEMS | STEPHACIDIN-A | MARINE SPONGE | ALKALOIDS | Dioxygenases - metabolism | Cyclization | Stereoisomerism | Aspergillus - enzymology | Aspergillus - metabolism | Indole Alkaloids - chemistry | Circular Dichroism | Indole Alkaloids - metabolism | Fungal Proteins - metabolism
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13. Full Text Fungal indole alkaloid biogenesis through evolution of a bifunctional reductase/Diels-Alderase
by Dan, QY and Newmister, SA and Klas, KR and Fraley, AE and McAfoos, TJ and Somoza, AD and Sunderhaus, JD and Ye, Y and Shende, VV and Yu, FA and Sanders, JN and Brown, WC and Zhao, L and Paton, RS and Houk, KN and Smith, JL and Sherman, DH and Williams, RM and Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
NATURE CHEMISTRY, ISSN 1755-4330, 11/2019, Volume 11, Issue 11, pp. 972 - 972
Prenylated indole alkaloids such as the calmodulin-inhibitory malbrancheamides and anthelmintic paraherquamides possess great structural diversity and... 
CORE | ENZYME | 4+2 CYCLOADDITION | BIOSYNTHESIS | PARAHERQUAMIDE | RING-SYSTEM | MALBRANCHEAMIDE | MARINE | CHEMISTRY, MULTIDISCIPLINARY | Reductases | Indole | Molecular dynamics | Homology | Enantiomers | Substrates | Intermediates | Alkaloids | Secondary metabolites | Cycloaddition | Mutagenesis | Metabolites | Biomimetics | Calcium-binding protein | Site-directed mutagenesis | NADP | Cascade chemical reactions | Calmodulin | Crystal structure | Reductase | Index Medicus
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14. Full Text Absolute Stereochemistry of Citrinadins A and B from Marine-Derived Fungus
by Mugishima, Takao and Tsuda, Masashi and Kasai, Yuu and Ishiyama, Haruaki and Fukushi, Eri and Kawabata, Jun and Watanabe, Masayuki and Akao, Kenichi and Kobayashi, Jun'ichi
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2005, Volume 70, Issue 23, pp. 9430 - 9435
Citrinadin A (2) is a pentacyclic indolinone alkaloid isolated from the cultured broth of a fungus, Penicillium citrinum, which was separated from a marine red... 
PENICILLIUM-ROQUEFORTI | METABOLITES | ASPERGILLUS-JAPONICUS JV-23 | X-RAY-ANALYSIS | PARAHERQUAMIDE | MARCFORTINE | CHEMISTRY, ORGANIC | OXINDOLE ALKALOIDS | DERIVATIVES | Valine - chemistry | Stereoisomerism | Valine - analogs & derivatives | Rhodophyta - chemistry | Circular Dichroism | Alkaloids - chemistry | Quinolizines - chemistry | Indole Alkaloids | Microbiological chemistry | Research | Red algae | Circular dichroism
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15. Full Text Synthetic studies toward paraherquamides E and F and related 13C-labeled putative biosynthetic intermediates: stereocontrolled synthesis of the α-alkyl-β-methylproline ring system
by Sommer, Konrad and Williams, Robert M
Tetrahedron, ISSN 0040-4020, 07/2008, Volume 64, Issue 30-31, pp. 7106 - 7111
A substituted 2R-allyl-3S-methylproline ethyl ester suitable for elaboration to paraherquamides E, F and related C-labeled putative biosynthesis intermediates... 
Paraherquamide | Asperparaline | Asymmetric synthesis | β-Methylproline
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16. Full Text Highly Stereoselective [4+2] and [3+2] Spiroannulations of 2‐(2‐Oxoindolin‐3‐ylidene)acetic Esters Catalyzed by Bifunctional Thioureas
by Monari, Magda and Montroni, Elisa and Nitti, Andrea and Lombardo, Marco and Trombini, Claudio and Quintavalla, Arianna
Chemistry – A European Journal, ISSN 0947-6539, 07/2015, Volume 21, Issue 31, pp. 11038 - 11049
A new Michael–Michael cascade reaction between 2‐(2‐oxoindolin‐3‐ylidene)acetic esters 1 and nitroenoates 2, catalyzed by bifunctional thioureas, is... 
Michael addition | organocatalysis | asymmetric catalysis | domino reactions | spiro compounds | Domino reactions | Asymmetric catalysis | Organocatalysis | Spiro compounds | ASYMMETRIC-SYNTHESIS | EFFICIENT SYNTHESIS | 6-MEMBERED SPIROCYCLIC OXINDOLES | CONSECUTIVE STEREOCENTERS | CHEMISTRY, MULTIDISCIPLINARY | CASCADE REACTION | BIOMIMETIC TOTAL-SYNTHESIS | SPIROOXINDOLE DERIVATIVES | PARAHERQUAMIDE CLASS | BAYLIS-HILLMAN CARBONATES | ENANTIOSELECTIVE TOTAL-SYNTHESIS | Catalysis | Thiourea - chemistry | Stereoisomerism | Indoles - chemistry | Spiro Compounds - chemistry | Nitro Compounds - chemistry | Esters | Analysis | Chemical industry | Carbon | Asymmetry | Catalysts | Strategy | Derivatives | Thioureas | Michael reaction
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17. Full Text Multicomponent Reaction to Construct Spirocyclic Oxindoles with a Michael (Triple Michael)/Cyclization Cascade Sequence as the Key Step
by Li, Jian and Wang, Ning and Li, Chunju and Jia, Xueshun
Chemistry – A European Journal, ISSN 0947-6539, 07/2012, Volume 18, Issue 31, pp. 9645 - 9650
Multicomponent cycloadditions with readily available isocyanides, allenoates, and isatylidene malononitriles are disclosed. This reaction, which does not... 
allenoates | Michael addition | multicomponent reactions | isocyanides | spiro compounds | MAMMALIAN-CELL CYCLE | ASPERGILLUS-FUMIGATUS | SPIROTRYPROSTATIN-B | PARAHERQUAMIDE | ENANTIOSELECTIVE CONSTRUCTION | CHEMISTRY, MULTIDISCIPLINARY | SPIROOXINDOLES | CYCLOADDITIONS | STEREOCENTERS | SYNTHETIC EFFICIENCY | Combinatorial Chemistry Techniques | Cyclization | Stereoisomerism | Spiro Compounds - chemical synthesis | Indoles - chemical synthesis | Molecular Structure | Piperazines - chemistry | Catalysis | Indoles - chemistry | Spiro Compounds - chemistry | Nitriles | Chemical properties | Cycloaddition | Cascades | Strategy | Malononitrile | Cleavage | Carbon | Bonding | Conversion
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18. Full Text Insecticidal Activity of Paraherquamides, Including Paraherquamide H and Paraherquamide I, Two New Alkaloids Isolated from Penicillium cluniae
by López-Gresa, M. Pilar and González, M. Carmen and Ciavatta, Letizia and Ayala, Ildefonso and Moya, Pilar and Primo, Jaime
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 04/2006, Volume 54, Issue 8, pp. 2921 - 2925
Paraherquamide H (1) and paraherquamide I (2), two new compounds of the paraherquamide (PHQ) family, together with the already known paraherquamide A (3),... 
Insecticide activity | Paraherquamide H | Penicillium cluniae | Paraherquamide I | Oncopeltus fasciatus | Brevianamides | Marcfortines | Paraherquamides | Diketopiperazines | diketopiperazines | METABOLITES | paraherquamide H | insecticide activity | ASPERGILLUS-JAPONICUS JV-23 | FOOD SCIENCE & TECHNOLOGY | paraherquamide I | MARCFORTINE | ABSOLUTE STEREOCHEMISTRY | ROQUEFORTI | brevianamides | paraherquamides | BIOSYNTHESIS | STEREOCONTROLLED TOTAL-SYNTHESIS | X-RAY-ANALYSIS | ASPERPARALINES | AGRICULTURE, MULTIDISCIPLINARY | ANTIPARASITIC AGENTS | CHEMISTRY, APPLIED | marcfortines | Animals | Magnetic Resonance Spectroscopy | Indolizines - chemistry | Mass Spectrometry | Insecticides | Molecular Structure | Penicillium - metabolism | Hemiptera | Spiro Compounds - chemistry
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19. Full Text Genome-Based Characterization of Two Prenylation Steps in the Assembly of the Stephacidin and Notoamide Anticancer Agents in a Marine-Derived Aspergillus sp
by Ding, Yousong and Wet, Jeffrey R. de and Cavalcoli, James and Li, Shengying and Greshock, Thomas J and Miller, Kenneth A and Finefield, Jennifer M and Sunderhaus, James D and McAfoos, Timothy J and Tsukamoto, Sachiko and Williams, Robert M and Sherman, David H
Journal of the American Chemical Society, ISSN 0002-7863, 09/2010, Volume 132, Issue 36, pp. 12733 - 12740
Stephacidin and notoamide natural products belong to a group of prenylated indole alkaloids containing a core bicyclo[2.2.2]diazaoctane ring system. These... 
SYNTHASE | BIOMIMETIC TOTAL-SYNTHESIS | AFLATOXIN | MALBRANCHEA-AURANTIACA | GENE-CLUSTER | PRENYLTRANSFERASES | BIOSYNTHESIS | PARAHERQUAMIDE | INDOLE ALKALOIDS | CHEMISTRY, MULTIDISCIPLINARY | FUMIGATUS | Prenylation | Stereoisomerism | Molecular Conformation | Antineoplastic Agents - chemistry | Aspergillus - metabolism | Antineoplastic Agents - metabolism | Animals | Aspergillus - genetics | Biological Factors - chemistry | Biological Factors - metabolism | Genome | Indole Alkaloids - chemistry | Indole Alkaloids - metabolism | Biological Factors - biosynthesis | Antimitotic agents | Alkaloids | Aspergillus | Indole | Physiological aspects | Genetic aspects | Chemical properties | Antineoplastic agents | Structure
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20. Full Text Concise Total Synthesis of (±)-Marcfortine B
by