Amanote Research
Register
Sign In
Synthesis and PKC Binding of a New Class of A-Ring Diversifiable Bryostatin Analogues Utilizing a Double Asymmetric Hydrogenation and Cross-Coupling Strategy
doi 10.1021/ol0618149.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Synthesis of Mepivacaine and Its Analogues by a Continuous-Flow Tandem Hydrogenation/Reductive Amination Strategy
European Journal of Organic Chemistry
Organic Chemistry
Theoretical Chemistry
Physical
Towards the Asymmetric Synthesis of Bryostatin 1
Pure and Applied Chemistry
Chemistry
Chemical Engineering
Synthesis and Utility of Ethylene (Meth)acrylate Copolymers Prepared by a Tandem Ring-Opening Polymerization Hydrogenation Strategy
Journal of Polymer Science, Part A: Polymer Chemistry
Organic Chemistry
Polymers
Materials Chemistry
Plastics
Taurine Analogues: A New Class of Therapeutics
Total Synthesis and Initial Biological Evaluation of New B-Ring-Modified Bryostatin Analogs
Synthesis of the Entire Framework of Tartrolon B Utilizing a Silicon-Tethered Ring-Closing Metathesis Strategy
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
A New and Effective Asymmetric Synthesis of 3-Phenylalkanals
Chemistry Letters
Chemistry
Enantioselective Total Synthesis of Brevetoxin A: Convergent Coupling Strategy and Completion
Chemistry - A European Journal
Organic Chemistry
Catalysis
Chemistry
Nonlinear Refractive Index Measurement Utilizing Bistable Behavior of Double Coupling Optical Fiber Ring Resonator
Photonic Sensors
Optics
Molecular Physics,
Optical
Atomic
Magnetic Materials
Electronic
