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References from Synthetic Approach to the ABCD Ring System of Anticancer Agent Fredericamycin A via Claisen Rearrangement and Ring-Closing Metathesis as Key Steps. Local targets link to admitted publications; unresolved targets remain external evidence.
In Vivo Investigation of the Roles of FdmM and FdmM1 in Fredericamycin Biosynthesis Unveiling a New Family of Oxygenases
10.1074/jbc.m109.014191 · 2009 · External reference
Fredericamycin A, a new antitumor antibiotic. I. Production, isolation and physicochemical properties
10.7164/antibiotics.34.1389 · 1981 · External reference
Fredericamycin A, an Antitumor Antibiotic of a Novel Skeletal Type
10.1021/ja00380a025 · 1982 · External reference
Biosynthesis of Fredericamycin A, a New Antitumor Antibiotic
10.1021/bi00323a035 · 1985 · External reference
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Identification of Fredericamycin E from Streptomyces griseus: Insights into Fredericamycin A Biosynthesis Highlighting Carbaspirocycle Formation
10.1021/np070664n · 2008 · External reference
Structure of Fredericamycin A, an antitumor antibiotic of a novel skeletal type; spectroscopic and mass spectral characterization
10.7164/antibiotics.40.786 · 1987 · External reference
Synthesis of Heterocyclic Compounds Related to Fredericamycin A-The Cyclopent[g] isoquinoline System
10.1002/jhet.5570240240 · 1987 · External reference
Fredericamycin A, a new antitumor antibiotic. II. Biological properties
10.7164/antibiotics.34.1402 · 1981 · External reference
Inhibition of topoisomerases by Fredericamycin A
10.1007/bf00300237 · 1989 · External reference
On the Formation of Oxygenated Radicals by Fredericamycin A and Implications to Its Anticancer Activity: An ESR Investigation
10.1021/bi00428a050 · 1989 · External reference
Unresolved reference
External reference
Magnetic Resonance Studies of Fredericamycin A: Evidence for oxygen-dependent Free-Radical Formation
10.1021/bi00367a028 · 2002 · External reference
Water soluble salts of Fredericamycin A: Preparation and biological activity
10.7164/antibiotics.41.976 · 1988 · External reference
Unresolved reference
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Total Synthesis of Natural and ent-Fredericamycin A
10.1021/ja00153a004 · 1995 · External reference
Unresolved reference
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Design and Semisynthesis of Novel Fredericamycin A Derivatives with an Improved Antitumor Profile
10.1016/j.bmcl.2006.03.029 · 2006 · External reference
Unresolved reference
External reference
Synthesis of (±)-fredericamycin A
10.1021/ja00227a030 · 1988 · External reference
Total Synthesis of Crystalline (±)-Fredericamycin A. Use of Radical Spirocyclization
10.1021/ja00104a009 · 1994 · External reference
Synthesis of (±)-Fredericamycin A
10.3987/com-93-s163 · 1994 · External reference
Asymmetric Total Synthesis of Fredericamycin A
10.1002/(sici)1521-3773(19990301)38:5<683::aid-anie683>3.0.co;2-0 · 1999 · External reference
Synthesis of (±)-fredericamycin A
10.1021/ja00282a042 · 1986 · External reference
NHC-Catalyzed Spiro Bis-Indane Formation via Domino Stetter-Aldol-Michael and Stetter-Aldol-Aldol Reactions
10.1021/ol102685u · 2010 · External reference
Methodology for the synthesis of the spiro[4.4]nonane system: an approach for the total synthesis of fredericamycin A
10.1039/c39840001119 · 1984 · External reference
Access to the Spiro hydrindandione ring system of Fredericamycin A through a Friedel-Crafts reaction
10.1016/s0040-4039(00)94933-5 · 1985 · External reference
Synthesis of (±)-Fredericamycin A
10.1021/ja00101a013 · 1994 · External reference
Synthesis of (±) Fredericamycin A
1987 · External reference
Enantiodivergent Synthesis of Either Enantiomer of ABCDE-Ring Analogue of Antitumor Antibiotic Fredericamycin A via Intramolecular [4 + 2] Cycloaddition Approach
10.1021/ol016696y · 2001 · External reference
10.1016/s0040-4039(01)93705-0
10.1016/s0040-4039(01)93705-0 · 1989 · External reference
Studies of the total synthesis of fredericamycin A. Preparation of key partial structures and development of an intermolecular alkyne-chromium carbene complex benzannulation cyclization approach to the ABCD(E) ring system
10.1021/jo00293a043 · 1990 · External reference
A Mercury-Mediated Acyl Migration in a Pinacol-Type Rearrangement. Model Studies toward the Synthesis of Fredericamycin A
10.1021/jo00355a036 · 1986 · External reference
Total Synthesis of (±)-Fredericamycin A. Use of Radical Spirocyclization
10.1039/c39920001489 · 1992 · External reference
Synthesis of the Spirocyclic Centre of Fredericamycin A by Phenoxy-Enoxy Radical Coupling
10.1016/s0040-4039(00)98619-2 · 1985 · External reference
Radical Spirocyclization: Synthesis of an Appropriately Oxygenated Spiro Compound Related to the Antitumor Antibiotic Fredericamycin A
10.1021/jo00383a032 · 1987 · External reference
Synthesis of (±) Fredericamycin A
10.1016/s0040-4039(00)77651-9 · 1993 · External reference
Model Studies Towards Fredericaycin A. Protocol for the Rapid Creation of the Spirocyclic Centre
10.1016/s0040-4039(00)95761-7 · 1987 · External reference
A Novel Synthesis of the Basic Carbon Framework of Fredericamycin A. Promising Routes for the Spiro Chiral Centre Construction of the CD-Ring System
10.1016/s0040-4039(01)80627-4 · 1989 · External reference
Model Studies Aimed at the Fredericamycin A. A Simple O-Quinodimethane Route to the Spiro Napthalene Portion
10.1016/s0040-4039(00)84427-5 · 1986 · External reference
Azadiene Diels-Alder Reactions. Total Synthesis of Natural and ent- Fredericamycin A
10.1002/jhet.5570330508 · 1996 · External reference
Palladium Catalyzed Cross-Coupling Acylation Approach to the Antitumor Antibiotic Fredericamycin A
10.1021/jo00112a067 · 1995 · External reference
The Diels–Alder Reaction in Total Synthesis
10.1002/1521-3773(20020517)41:10<1668::aid-anie1668>3.0.co;2-z · 2002 · External reference
Diversity-Oriented Approaches to Polycyclics and Bioinspired Molecules via the Diels–Alder Strategy: Green Chemistry, Synthetic Economy, and Beyond
10.1021/co500146u · 2015 · External reference
Design and synthesis of oxa-bowls via Diels–Alder reaction and ring-rearrangement metathesis as key steps
10.1016/j.tetlet.2014.08.108 · 2014 · External reference
Catalytic Enantioselective Diels–Alder Reactions: Methods, Mechanistic Fundamentals, Pathways, and Applications
10.1002/1521-3773(20020517)41:10<1650::aid-anie1650>3.0.co;2-b · 2002 · External reference
10.1002/9783527610549
10.1002/9783527610549 · 2007 · External reference
A synergistic approach to polycyclics via a strategic utilization of Claisen rearrangement and olefin metathesis
10.1039/c1ob05413a · 2011 · External reference
Claisen Rearrangement over the Past Nine Decades
10.1021/cr020703u · 2004 · External reference
Microwave-assisted Claisen Rearrangement on a Silica gel Support
10.1016/j.tetlet.2004.11.012 · 2004 · External reference
A new protocol for benzoannulation by double Claisen rearrangement and ring-closing metathesis reactions as key steps
10.1016/j.tetlet.2004.01.149 · 2004 · External reference
10.1002/9783527674107
10.1002/9783527674107 · 2015 · External reference
Synthesis of Diverse Polycyclic Compounds via Catalytic Metathesis
10.1055/s-2007-990954 · 2007 · External reference
Strategies and tactics in olefin metathesis
10.1016/j.tet.2011.10.018 · 2012 · External reference
Synthesis of conformationally constrained α-amino acid derivatives using ethyl isocyanoacetate as glycine equivalent
10.1016/s0960-894x(97)10075-0 · 1997 · External reference
Spiro-annulation via ring-closing metathesis reaction
10.1055/s-1999-2896 · 1999 · External reference
Retro-Diels-Alder Strategy in Natural Product Synthesis
10.1055/s-1987-27894 · 1987 · External reference
A new synthetic strategy to 2,3-diallyl-1,4-quinones via one-pot double Claisen rearrangement and retro Diels–Alder reaction
10.1016/j.tetlet.2016.05.101 · 2016 · External reference
Recent developments in the retro-Diels–Alder reaction
10.1039/c3ra22762f · 2013 · External reference
A Synthetic Approach to Polycyclic Hydroaromatic Systems Related to the 19-Norsteroids
10.1021/ja01558a058 · 1957 · External reference
Synthetic Studies on Kinamycin Antibiotics: Synthesis of a Trioxygenated Benz[f]indenone and its Diels ± Alder Reaction to a Kinamycin Skeleton
10.1002/1522-2675(200204)85:4<1186::aid-hlca1186>3.0.co;2-q · 2002 · External reference
Diels–Alder reactions using 4,7-dioxygenated indanones as dienophiles for regioselective construction of oxygenated 2,3-dihydrobenz[f]indenone skeleton
10.3762/bjoc.4.15 · 2008 · External reference
The Synthesis of Analogs of the Hallucinogen 1-(2,5-Dimethoxy-4-methylphenyl)-2-aminopropane (DOM). II. Some Ring-methoxylated 1-Amino-and 2-Aminoindanes
10.1139/v74-061 · 1974 · External reference
Synthesis and Rearrangement of Cage [4.3.2]Propellanes that Contain a Spiro Linkage
10.1002/ejoc.201700617 · 2017 · External reference
Synthetic approach to Oxa-cage systems via Ring-Closing Metathesis
10.3987/com-18-s(t)83 · 2018 · External reference
2,3-Dimethoxycinnamic acid
1963 · External reference
Unexpected regioselectivity observed in the bromination and epoxidation reactions of p-benzoquinone-fused norbornadiene: An experimental and computational study
10.1016/j.tet.2017.02.017 · 2017 · External reference
Protecting-Group-Free-Synthesis
10.1055/s-2006-950311 · 2006 · External reference
