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References from Unconventional Macrocyclizations in Natural Product Synthesis. Local targets link to admitted publications; unresolved targets remain external evidence.
Bioactive Macrocycles from Nature
2015 · External reference
Macrocycles in New Drug Discovery
10.4155/fmc.12.93 · 2012 · External reference
Macrocycles Are Great Cycles: Applications, Opportunities, and Challenges of Synthetic Macrocycles in Drug Discovery
10.1021/jm1012374 · 2011 · External reference
The Exploration of Macrocycles for Drug Discovery - an Underexploited Structural Class
10.1038/nrd2590 · 2008 · External reference
Design, Properties and Recent Application of Macrocycles in Medicinal Chemistry
10.2533/chimia.2017.678 · 2017 · External reference
Macrocycles: Lessons from the Distant Past, Recent Developments, and Future Directions
10.1039/c4sc03089c · 2015 · External reference
Macrocyclization Reactions: The Importance of Conformational, Configurational, and Template-Induced Preorganization
10.1021/acs.chemrev.5b00056 · 2015 · External reference
Conformation-Directed Macrocyclization Reactions
10.1002/ejoc.200400751 · 2005 · External reference
Stereoconfining Macrocyclizations in the Total Synthesis of Natural Products
10.1039/c8np00094h · 2019 · External reference
Ring-Closing Metathesis and Related Processes in Organic Synthesis
10.1021/ar00059a002 · 1995 · External reference
Macrocyclization by Ring-Closing Metathesis in the Total Synthesis of Natural Products: Reaction Conditions and Limitations
10.1002/anie.200600641 · 2006 · External reference
The Remarkable Metal-Catalysed Olefin Metathesis Reaction
10.1038/nature06351 · 2007 · External reference
Update 1 of: Macrolactonizations in the Total Synthesis of Natural Products
10.1021/cr300129n · 2013 · External reference
Catalytic Macrolactonizations for Natural Product Synthesis
10.1039/c7np00038c · 2017 · External reference
The Cyclization of Peptides and Depsipeptides
10.1002/psc.491 · 2003 · External reference
Amide Bond Formation and Peptide Coupling
10.1016/j.tet.2005.08.031 · 2005 · External reference
Alternative Strategies for the Construction of Macrocycles
10.1002/9781119092599.ch13 · 2017 · External reference
The Synthetic Challenge of Diazonamide A, a Macrocyclic Indole Bis-Oxazole Marine Natural Product
10.1039/b705663j · 2008 · External reference
Isolation and Structure Determination of Diazonamides A and B, Unusual Cytotoxic Metabolites from the Marine Ascidian Diazona Chinensis
10.1021/ja00006a060 · 1991 · External reference
Total Synthesis of Nominal Diazonamides– Part 1: Convergent Preparation of the Structure Proposed for (−)-Diazonamide A
10.1002/1521-3773(20011217)40:24<4765::aid-anie4765>3.0.co;2-1 · 2001 · External reference
Total Synthesis of Nominal Diazonamides– Part 2: On the True Structure and Origin of Natural Isolates
10.1002/1521-3773(20011217)40:24<4770::aid-anie4770>3.0.co;2-t · 2001 · External reference
Progress toward Synthesis of Diazonamide A. Preparation of a 3-(Oxazol-5-Yl)-4-Trifluoromethyl-Sulfonyloxyindole and Its Use in Biaryl Coupling Reactions
10.1021/ol005548p · 2000 · External reference
Construction of the Complete Aromatic Core of Diazonamide A by a Novel Hetero Pinacol Macrocyclization Cascade Reaction
10.1002/1521-3773(20011217)40:24<4705::aid-anie4705>3.0.co;2-d · 2001 · External reference
Total Synthesis of Diazonamide A
10.1002/1521-3773(20020916)41:18<3495::aid-anie3495>3.0.co;2-7 · 2002 · External reference
Chemistry and Biology of Diazonamide A: First Total Synthesis and Confirmation of the True Structure
10.1021/ja040092i · 2004 · External reference
A Concise and Flexible Total Synthesis of (−)-Diazonamide A
10.1002/anie.200352577 · 2003 · External reference
The Second Total Synthesis of Diazonamide A
10.1002/anie.200351112 · 2003 · External reference
Chemistry and Biology of Diazonamide A: Second Total Synthesis and Biological Investigations
10.1021/ja040093a · 2004 · External reference
Total Synthesis of Diazonamide A
10.1039/c0sc00577k · 2011 · External reference
An Expedient Formal Total Synthesis of (−)-Diazonamide A via a Powerful, Stereoselective O-Aryl to C-Aryl Migration to Form the C10 Quaternary Center
10.1021/ja0744448 · 2007 · External reference
A Concise Formal Synthesis of Diazonamide a by the Stereoselective Construction of the C10 Quaternary Center
10.1002/anie.200906318 · 2010 · External reference
Formal Total Synthesis of Diazonamide A by Indole Oxidative Rearrangement
10.1002/chem.201601605 · 2016 · External reference
Unresolved reference
2010 · External reference
Organic Syntheses by Beans of Noble Metal Compounds XVII. Reaction of π-Allylpalladium Chloride with Nucleophiles
10.1016/s0040-4039(00)71674-1 · 1965 · External reference
Arylation, Methylation, and Carboxyalkylation of Olefins by Group VIII Metal Derivatives
10.1021/ja01022a034 · 1968 · External reference
The Arylation of Allylic Alcohols with Organopalladium Compounds. A New Synthesis of 3-Aryl Aldehydes and Ketones
10.1021/ja01022a035 · 1968 · External reference
Aromatic Haloethylation with Palladium and Copper Halides
10.1021/ja01022a038 · 1968 · External reference
The Addition of Alkyl- and Arylpalladium Chlorides to Conjugated Dienes
10.1021/ja01022a039 · 1968 · External reference
A Novel Stereospecific Alkenyl-Alkenyl Cross-Coupling by a Palladium- or Nickel-Catalyzed Reaction of Alkenylalanes with Alkenyl Halides
10.1021/ja00437a067 · 1976 · External reference
Novel Stereoselective Alkenyl-Aryl Coupling via Nickel-Catalysed Reaction of Alkenylalanes with Aryl Halides
10.1039/c3976000596b · 1976 · External reference
Stereoselective Synthesis of Arylated (E)-Alkenes by the Reaction of Alk-1 -Enylboranes with Aryl Halides in the Presence of Palladium Catalyst
10.1039/c39790000866 · 1979 · External reference
New Synthetic Reactions. Allylic Alkylation
10.1021/ja00782a080 · 1973 · External reference
Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
10.1021/cr020027w · 2003 · External reference
The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry
10.1021/cr050992x · 2007 · External reference
The Stille Reaction, 38 Years Later
10.1021/acscatal.5b00448 · 2015 · External reference
Palladium-Catalyzed Synthesis of Macrocycles
10.1002/9781119092599.ch12 · 2017 · External reference
A General, Selective, and Facile Method for Ketone Synthesis from Acid Chlorides and Organotin Compounds Catalyzed by Palladium
10.1021/ja00479a077 · 1978 · External reference
The Palladium-Catalyzed Cross-Coupling Reactions of Organotin Reagents with Organic Electrophiles
10.1002/anie.198605081 · 1986 · External reference
Reactions of Allyltin Compounds III. Allylation of Aromatic Halides with Allyltributyltin in the Presence of Tetrakis(Triphenylphosphine)Palladium(0)
10.1246/cl.1977.301 · 1977 · External reference
Alkylation, Arylation, and Vinylation of Acyl Chlorides by Means of Organotin Compounds in the Presence of Catalytic Amounts of Tetrakis(Triphenylphosphine)Palladium(0)
10.1246/cl.1977.1423 · 1977 · External reference
The Intramolecular Stille Reaction in Some Target Natural Product Syntheses
10.1016/s0022-328x(02)01169-5 · 2002 · External reference
Total Synthesis of (±)-Epi-Jatrophone and (±)-Jatrophone Using Palladium-Catalyzed Carbonylative Coupling of Vinyl Triflates with Vinylstannanes as the Macrocycle-Forming Step
10.1021/ja00179a035 · 1990 · External reference
Total Synthesis of Chivosazole F
10.1021/ja107290s · 2010 · External reference
Total Syntheses of the Thiopeptides Amythiamicin C and D
10.1002/chem.201002144 · 2010 · External reference
Total Synthesis of Nannocystin Ax
10.1039/c7cc00469a · 2017 · External reference
Total Synthesis of Rapamycin
10.1021/ja00063a093 · 1993 · External reference
Total Syntheses of (−)-Macrolactin A, (+)-Macrolactin E, and (−)-Macrolactinic Acid: An Exercise in Stille Cross-Coupling Chemistry
10.1021/ja980203b · 1998 · External reference
Total Synthesis of (−)-Sarain A
10.1002/anie.200600417 · 2006 · External reference
The Heck Reaction as a Sharpening Stone of Palladium Catalysis
10.1021/cr9903048 · 2000 · External reference
Formal Total Synthesis of Palmerolide A
10.1055/s-0029-1216921 · 2009 · External reference
Total Synthesis of the Originally Proposed and Revised Structures of Palmerolide A
10.1002/anie.200702243 · 2007 · External reference
Total Synthesis of the Marine Natural Product Solomonamide B Necessitates Stereochemical Revision
10.1021/acs.orglett.6b01395 · 2016 · External reference
Total Synthesis of the Potent Anti-Inflammatory Natural Product Solomonamide A along with Structural Revision and Biological Activity Evaluation
10.1039/c8ob02713g · 2018 · External reference
Total Synthesis of Etnangien
10.1021/ja9056163 · 2009 · External reference
Total Synthesis of Archazolid A
10.1021/ja071461o · 2007 · External reference
Stereoselective Total Synthesis of Bioactive Marine Natural Product Biselyngbyolide B
10.1021/acs.orglett.6b00713 · 2016 · External reference
Access to the Enantiopure Axially Chiral Cyclophane Isoplagiochin D through Atropo-Diastereoselective Heck Coupling
10.1002/anie.201803677 · 2018 · External reference
Atroposelective Heck Macrocyclization: Enantioselective Synthesis of Bis(Bibenzylic) Natural Products
10.1021/ol302132s · 2012 · External reference
Formal Total Synthesis of Oximidine II via a Suzuki-Type Cross-Coupling Macrocyclization Employing Potassium Organotrifluoroborates
10.1021/ja047190o · 2004 · External reference
Total Synthesis of (+)-Superstolide A
10.1021/jo801794s · 2008 · External reference
Intramolecular Suzuki-Miyaura Reaction for the Total Synthesis of Signal Peptidase Inhibitors, Arylomycins A2 and B2
10.1002/chem.201000924 · 2010 · External reference
Total Synthesis of Rhizopodin
10.1002/anie.201201946 · 2012 · External reference
Concise Total Synthesis of Nannocystin A
10.1002/anie.201606679 · 2016 · External reference
Total Synthesis of (+)-Phomactin A Using a B-Alkyl Suzuki Macrocyclization
10.1021/ja0296531 · 2003 · External reference
A Two-Step, Three-Component Synthesis of PGE1: Utilization of α-Iodoenones in Pd(0)-Catalyzed Cross-Couplings of Organoboranes
10.1021/ja00076a079 · 1993 · External reference
Isocomplestatin: Total Synthesis and Stereochemical Revision
10.1021/ja051790l · 2005 · External reference
Total Synthesis of Anti-HIV Agent Chloropeptin I
10.1021/ja030249r · 2003 · External reference
A Domino 10-Step Total Synthesis of FR252921 and Its Analogues, Complex Macrocyclic Immunosuppressants
10.1021/jacs.9b07185 · 2019 · External reference
Synthesis of a Promising Immunosuppressant: FR252921
10.1021/ol702110k · 2007 · External reference
Synthesis of Two Bioactive Natural Products: FR252921 and Pseudotrienic Acid B
10.1002/chem.200802649 · 2009 · External reference
Dual Catalysis Becomes Diastereodivergent
10.1002/anie.201305933 · 2013 · External reference
Diastereodivergent Processes in Palladium-Catalyzed Allylic Alkylation
10.1002/cctc.201200644 · 2013 · External reference
Cyclobutenes: At a Crossroad between Diastereoselective Syntheses of Dienes and Unique Palladium-Catalyzed Asymmetric Allylic Substitutions
10.1021/acs.accounts.6b00375 · 2016 · External reference
Total Synthesis of Humulene. A Stereoselective Approach
10.1021/ja00453a069 · 1977 · External reference
Total Synthesis of Roseophilin
10.1021/ja973846k · 1998 · External reference
Total Synthesis of (+)-Macquarimicin A
10.1021/ja038732p · 2003 · External reference
Transannular Diels-Alder Route to Systems Related to Dynemicin A
10.1021/ja00176a060 · 1990 · External reference
Efficient Construction of the Kedarcidin Chromophore Ansamacrolide
10.1021/ol0477374 · 2005 · External reference
Total Synthesis of Bryostatin 16 Using Atom-Economical and Chemoselective Approaches
10.1038/nature07543 · 2008 · External reference
Total Synthesis and Stereochemical Assignment of Streptide
10.1021/jacs.9b09067 · 2019 · External reference
Zur Reaktionsweise Des Pentaphenyl-Phosphors Und Einiger Derivate
10.1002/jlac.19535800107 · 1953 · External reference
Über Triphenyl-Phosphin-Methylene Als Olefinbildende Reagenzien (I. Mitteil.)
10.1002/cber.19540870919 · 1954 · External reference
Über Triphenyl-Phosphinmethylene Als Olefinbildende Reagenzien (II. Mitteil.)
10.1002/cber.19550881110 · 1955 · External reference
Synthesis and Revised Structure of Garuganin III
10.1021/jo00076a036 · 1993 · External reference
(+)-Trienomycins A, B, C, and F and (+)-Mycotrienins I and II: Relative and Absolute Stereochemistry
10.1021/ja961400i · 1996 · External reference
Total Syntheses of (+)-Trienomycins A and F via a Unified Strategy
10.1021/ja961401a · 1996 · External reference
Phosphororganische Verbindungen, XII. Phosphinoxyde Als Olefinierungsreagenzien
10.1002/cber.19580910113 · 1958 · External reference
Phosphororganische Verbindungen, XX. Phosphinoxyde Als Olefinierungsreagenzien
10.1002/cber.19590921017 · 1959 · External reference
The Utility of Phosphonate Carbanions in Olefin Synthesis
10.1021/ja01468a042 · 1961 · External reference
Direct Synthesis of Z-Unsaturated Esters. A Useful Modification of the Horner-Emmons Olefination
10.1016/s0040-4039(00)85909-2 · 1983 · External reference
A New Synthesis of Olefins from Carbonyl Compounds and Phoshonic Acid Bis Amides
10.1021/ja01026a045 · 1968 · External reference
Practical Synthesis of Z-Unsaturated Esters by Using a New Horner-Emmons Reagent, Ethyl Diphenylphosphonoacetate
10.1016/0040-4039(95)00726-s · 1995 · External reference
Highly Selective Synthesis of Z -Unsaturated Esters by Using New Horner–Emmons Reagents, Ethyl (Diarylphosphono)Acetates
10.1021/jo970057c · 1997 · External reference
Total Synthesis of Natural (+)-Lasonolide A
10.1002/anie.200352016 · 2003 · External reference
Total Synthesis of (+)-Dactylolide
10.1021/ol051040g · 2005 · External reference
Asymmetric Reduction of Aromatic Ketones with Chiral Alkoxy-Amine-Borane Complexes
10.1039/c39810000315 · 1981 · External reference
Asymmetric Reduction of Aromatic Ketones with the Reagent Prepared from (S)-(−)-2-Amino-3-Methyl-1,1-Diphenylbutan-1-Ol and Borane
10.1039/c39830000469 · 1983 · External reference
Highly Enantioselective Borane Reduction of Ketones Catalyzed by Chiral Oxazaborolidines. Mechanism and Synthetic Implications
10.1021/ja00252a056 · 1987 · External reference
A Stable and Easily Prepared Catalyst for the Enantioselective Reduction of Ketones: Applications to Multistep Syntheses
10.1021/ja00259a075 · 1987 · External reference
C–H Functionalization Logic in Total Synthesis
10.1039/c0cs00182a · 2011 · External reference
Recent Developments in Natural Product Synthesis Using Metal-Catalysed C–H Bond Functionalisation
10.1039/c1cs15013h · 2011 · External reference
Total Synthesis of (+)-Complanadine A Using an Iridium-Catalyzed Pyridine C–H Functionalization
10.1021/ja101893b · 2010 · External reference
Total Synthesis and Structural Revision of the Piperarborenines via Sequential Cyclobutane C–H Arylation
10.1021/ja209205x · 2011 · External reference
C–H Bond Arylation in the Synthesis of Aryltetralin Lignans: A Short Total Synthesis of Podophyllotoxin
10.1002/anie.201311112 · 2014 · External reference
C–H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity
10.1002/anie.201804551 · 2018 · External reference
Synthesis of Diaryl Ethers through the Copper-Promoted Arylation of Phenols with Arylboronic Acids. An Expedient Synthesis of Thyroxine
10.1016/s0040-4039(98)00502-4 · 1998 · External reference
Synthesis and Conformational Properties of the M(4–6)(5–7) Bicyclic Tetrapeptide Common to the Vancomycin Antibiotics
10.1021/ja964419u · 1997 · External reference
Scalable Access to Arylomycins via C-H Functionalization Logic
10.1021/jacs.8b00087 · 2018 · External reference
The Diels-Alder Reaction in Total Synthesis K
10.1002/1521-3773(20020517)41:10<1668::aid-anie1668>3.0.co;2-z · 2002 · External reference
A Simplified Total Synthesis of Cytochalasins via an Intramolecular Diels-Alder Reaction
10.1021/ja00354a072 · 1983 · External reference
An Intramolecular Diels-Alder Approach to the Synthesis of Chlorothricolide. Synthesis of (±)-24–0-Methylchlorothricolide
10.1021/jo00298a003 · 1990 · External reference
Total Synthesis of Pinnatoxin A
10.1021/ja981257o · 1998 · External reference
A Diels–Alder Macrocyclization Enables an Efficient Asymmetric Synthesis of the Antibacterial Natural Product Abyssomicin C
10.1002/anie.200502119 · 2005 · External reference
Enantioselective Total Synthesis of Isoedunol and β-Araneosene Featuring Unconventional Strategy and Methodology
10.1021/ja055137+ · 2005 · External reference
Total Synthesis of (±)-Haouamine A
10.1021/ja0602997 · 2006 · External reference
Total Synthesis of (±)-Cavicularin: Control of Pyrone Diels-Alder Regiochemistry Using Isomeric Vinyl Sulfones
10.1021/ol303390a · 2013 · External reference
Total Synthesis of Sporolide B
10.1002/anie.200900264 · 2009 · External reference
Application of the Allylic Diazene Rearrangement: Synthesis of the Enediyne-Bridged Tricyclic Core of Dynemicin A
10.1021/ja00040a085 · 1992 · External reference
Total Syntheses of Di- and Tri-O-Methyl Dynemicin A Methyl Esters
10.1021/ja00075a071 · 1993 · External reference
Synthesis and Absolute Stereochemical Assignment of (+)-Miyakolide
10.1021/ja990789h · 1999 · External reference
Remote Stereoinductive Intramolecular Nitrile Oxide Cycloaddition: Asymmetric Total Synthesis and Structure Revision of (−)-11β-Hydroxycurvularin
10.1021/acs.joc.5b02760 · 2016 · External reference
Unique Structural Topology and Reactivities of the ABD Tricycle in Phomactin A
10.1039/b511338e · 2005 · External reference
Intramolecular Formal Oxa-[3 + 3] Cycloaddition Approach to the ABD System of Phomactin A
10.1021/ol030115i · 2003 · External reference
Catalyst-Controlled Selective Functionalization of Unactivated C-H Bonds in the Presence of Electronically Activated C-H Bonds
10.1021/jacs.8b07534 · 2018 · External reference
Synthesis of 10-Membered and Larger Rings via Free Radical Methods
10.1016/j.tet.2018.01.056 · 2018 · External reference
Pinacol Coupling Reactions
10.1016/b978-0-08-097742-3.00316-5 · 2014 · External reference
Total Synthesis of (±)-Crassin by Titanium-Induced Pinacol Coupling
10.1021/ja00206a031 · 1989 · External reference
The McMurry Coupling and Related Reactions
10.1002/0471264180.or082.01 · 2013 · External reference
Synthesis of the (9S,18R) Diastereomer of Cyclamenol A
10.1002/(sici)1521-3773(20000317)39:6<1125::aid-anie1125>3.0.co;2-o · 2000 · External reference
The Witkop Cyclization: A Photoinduced C-H Activation of the Indole System
10.1002/anie.201307391 · 2014 · External reference
The Synthesis of Garugamblin-1
10.1016/s0040-4020(01)80406-3 · 1993 · External reference
Macrocyclization through Radical-Mediated Vinylcyclopropane/Alkene Condensation. Facile Entry into the Brefeldin Ring System
10.1021/jo00076a056 · 1993 · External reference
Total Synthesis of (−)-Epothilone A
10.1002/anie.199628011 · 1996 · External reference
Total Syntheses of Epothilones A and B
10.1021/ja971946k · 1997 · External reference
Total Synthesis of Rapamycin via a Novel Titanium-Mediated Aldol Macrocyclization Reaction
10.1021/ja00073a083 · 1993 · External reference
Synthesis of a Protected (±)-Calicheamicinone Derivative by Sequential Introduction of Functionality into the Bicyclo[7.3.1]Enediyne Core Structure
10.1021/ja970743t · 1997 · External reference
Unresolved reference
2014 · External reference
Asymmetric Total Synthesis of (−)-Cebulactam A1
10.1039/c3qo00036b · 2014 · External reference
The Remarkable Journey of Catalysts from Stoichiometric to Catalytic Quantity for Allyltrimethylsilane Inspired Allylation of Acetals, Ketals, Aldehydes and Ketones
10.1039/c6ra27813b · 2017 · External reference
Prins-Type Cyclization Reactions in Natural Product Synthesis
10.1002/ejoc.201201557 · 2013 · External reference
Efficient Synthetic Access to a New Family of Highly Potent Bryostatin Analogues via a Prins-Driven Macrocyclization Strategy
10.1021/ja8015632 · 2008 · External reference
Scalable Synthesis of Bryostatin 1 and Analogs, Adjuvant Leads against Latent HIV
10.1126/science.aan7969 · 2017 · External reference
Recent Efforts to Construct the B-Ring of Bryostatins
10.1039/c3cc45947k · 2013 · External reference
Total Synthesis of the Cyanolide A Aglycon
10.1021/ja204228q · 2011 · External reference
Total Synthesis of the Spirocyclic Imine Marine Toxin (−)-Gymnodimine and an Unnatural C4-Epimer
10.1021/ja207385y · 2011 · External reference
Total Synthesis of Calicheamicinone: New Arrangements for Actuation of the Reductive Cycloaromatization of Aglycon Congeners
10.1021/ja00010a030 · 1991 · External reference
A Convergent Total Synthesis of Calicheamicin γI1
10.1002/anie.199408581 · 1994 · External reference
Total Synthesis of (+)-Neocarzinostatin Chromophore
10.1021/ja980588y · 1998 · External reference
Total Synthesis of Calicheamicin γI1. 1. Synthesis of the Oligosaccharide Fragment
10.1021/ja00070a004 · 1993 · External reference
Carbon-Carbon Bond Formations Involving Organochromium(III) Reagents
10.1021/cr9703360 · 1999 · External reference
A Nozaki-Hiyama-Kishi Ni(II)/Cr(II) Coupling Approach to the Phomactins
10.1021/ol015807q · 2001 · External reference
A Macrocyclic β-Iodoallenolate Intermediate Is Key: Synthesis of the ABD Core of Phomactin A
10.1021/ol3017116 · 2012 · External reference
Development of a Highly α-Regioselective Metal-Mediated Allylation Reaction in Aqueous Media: New Mechanistic Proposal for the Origin of α-Homoallylic Alcohols
10.1021/ja029276s · 2003 · External reference
Total Syntheses of the Resorcylic Acid Lactones Paecilomycin F and Cochliomycin C Using an Intramolecular Loh-Type α-Allylation Reaction for Macrolide Formation
10.1021/acs.orglett.6b01963 · 2016 · External reference
A Comparative Analysis of the Total Syntheses of the Amphidinolide T Natural Products
10.1039/b507315b · 2005 · External reference
Enantioselective Synthesis of (−)-Terpestacin and Structural Revision of Siccanol Using Catalytic Stereoselective Fragment Couplings and Macrocyclizations
10.1021/ja0470968 · 2004 · External reference
Nickel-Catalyzed Cyclizations, Couplings, and Cycloadditions Involving Three Reactive Components
10.1021/ar990095d · 2000 · External reference
New N- and O-Arylations with Phenylboronic Acids and Cupric Acetate
10.1016/s0040-4039(98)00503-6 · 1998 · External reference
Synthesis of Diaryl Ethers through the Copper-Promoted Arylation of Phenols with Arylboronic Acids. An Expedient Synthesis of Thyroxine
10.1016/s0040-4039(98)00502-4 · 1998 · External reference
New Aryl/Heteroaryl C─N Bond Cross-Coupling Reactions via Arylboronic Acid/Cupric Acetate Arylation
10.1016/s0040-4039(98)00504-8 · 1998 · External reference
Total Synthesis of (+)-Piperazinomycin
10.1021/ja00077a047 · 1993 · External reference
Total Synthesis of Hirsutellone B via Ullmann-Type Direct 13-Membered Macrocyclization
10.1021/ol202748e · 2011 · External reference
Total Synthesis of Hirsutellone B
10.1002/anie.200903382 · 2009 · External reference
Catalytic Macrocyclization Strategies Using Continuous Flow: Formal Total Synthesis of Ivorenolide A
10.1021/acs.joc.6b01500 · 2016 · External reference
Isolation, Synthesis and Bioactivity Studies of Phomactin Terpenoids
10.1038/s41557-018-0084-x · 2018 · External reference
A Corey–Seebach Macrocyclisation Strategy for the Synthesis of Riccardin C and an Unnatural Macrocyclic Bis(Bibenzyl) Analogue
10.1002/ejoc.201601179 · 2016 · External reference
