Amanote Research
Register
Sign In
A Total Synthesis of Xestadecalactone a and Proof of Its Absolute Stereochemistry: Interesting Observations on Dienophilic Control With 1, 3-Disubstituted Nonequivalent Allenes
doi 10.1021/ja064270e.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Synthesis of Ring a of Ambruticin and Proof of Its Absolute Stereochemistry
Canadian Journal of Chemistry
Organic Chemistry
Catalysis
Chemistry
Control of Stereochemistry: A General Synthesis of Cis- Or Trans-B, G-Disubstituted-G-Butyrolactones Following Z-Crotylboration
Total Synthesis of Amidepsine B and Revision of Its Absolute Configuration
Journal of Antibiotics
Drug Discovery
Pharmacology
Copper Hydride-Catalyzed Enantioselective Synthesis of Axially Chiral 1,3-Disubstituted Allenes
The First Total Synthesis of Sphingofungin E and the Determination of Its Stereochemistry
Synlett
Organic Chemistry
Copper Hydride Catalyzed Enantioselective Synthesis of Axially Chiral 1,3-Disubstituted Allenes
Total Synthesis, Structural Revision, and Absolute Configuration of (+)-Clavosolide A
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Relative and Absolute Configuration of Allohedycaryol. Enantiospecific Total Synthesis of Its Enantiomer
Journal of Organic Chemistry
Organic Chemistry
Concise Formal Synthesis of (+)-Englerin a and Total Synthesis of (-)-Orientalol F: Establishment of the Stereochemistry of the Organocatalytic [4+3]-Cycloaddition Reaction
Synlett
Organic Chemistry
