Total Synthesis of the Annonaceous Acetogenins Asiminocin and Asiminecin by a Bidirectional Approach
- 1 August 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (17) , 5996-6000
- https://doi.org/10.1021/jo970424k
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Total Synthesis of the Annonaceous Acetogenin (+)-Asimicin. Development of a New Bidirectional StrategyThe Journal of Organic Chemistry, 1997
- Amination, Aminocarbonylation, and Alkoxycarbonylation of Allenic/Propargylic Pd Intermediates Derived from Nonracemic Propargylic Mesylates: Synthesis of Nonracemic Propargyl Amines, Allenic Amides, and ButenolidesThe Journal of Organic Chemistry, 1996
- An Efficient Bidirectional Approach to the C2-Symmetric Stereoisomers of the Bistetrahydrofuran Core of the AcetogeninsThe Journal of Organic Chemistry, 1996
- Synthesis of a C22-34 Subunit of the Immunosuppressant FK-506The Journal of Organic Chemistry, 1995
- Synthesis of Furans and 2,5-Dihydrofurans by Ag(I)-Catalyzed Isomerization of Allenones, Alkynyl Allylic Alcohols, and AllenylcarbinolsThe Journal of Organic Chemistry, 1995
- Synthesis of (+)-(15,16,19,20,23,24)-hexepi-uvaricin: a bis(tetrahydrofuranyl) annonaceous acetogenin analogJournal of the American Chemical Society, 1991
- On the 1,3-isomerization of nonracemic .alpha.-(alkoxy)allylstannanesJournal of the American Chemical Society, 1991
- Total synthesis of (.+-.)-lythrancepine II and (.+-.)-lythrancepine IIIThe Journal of Organic Chemistry, 1987
- On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcoholsThe Journal of Organic Chemistry, 1986
- Selective reductions. 26. Lithium triethylborohydride as an exceptionally powerful and selective reducing agent in organic synthesis. Exploration of the reactions with selected organic compounds containing representative functional groupsThe Journal of Organic Chemistry, 1980