Cart
Research Article
Total Synthesis of Aegyptinones A and B
Hi-Res PDFPurchase the full-text
- PDF/HTML,
figures/images,
references and tables,
(where available)
Note: In lieu of an abstract, this is the article's first page.
Citing Articles
Citation data is made available by participants in CrossRef's Cited-by Linking service. For a more comprehensive list of citations to this article, users are encouraged to perform a search in SciFinder.
This article has been cited by 7 ACS Journal articles (5 most recent appear below).
Synthesis of Polycyclic Benzofused Nitrogen Heterocycles via a Tandem Ynamide Benzannulation/Ring-Closing Metathesis Strategy. Application in a Formal Total Synthesis of (+)-FR900482
Xiao Yin Mak, Aimee L. Crombie, and Rick L. DanheiserThe Journal of Organic Chemistry2011 76 (6), 1852-1873Synthesis of Polycyclic Benzofused Nitrogen Heterocycles via a Tandem Ynamide Benzannulation/Ring-Closing Metathesis Strategy. Application in a Formal Total Synthesis of (+)-FR900482
Xiao Yin Mak, Aimee L. Crombie, and Rick L. DanheiserThe Journal of Organic Chemistry2011 76 (6), 1852-1873A two-stage “tandem strategy” for the synthesis of benzofused nitrogen heterocycles is described that is particularly useful for the construction of systems with a high level of substitution on the benzenoid ring. The first stage in the strategy involves ...
Diastereoselective Diels−Alder Reactions with an Allenyl-Containing Spiro-Amido Chiral Auxiliary
Jeff R. Henderson, Julian P. Chesterman, Masood Parvez and Brian A. KeayThe Journal of Organic Chemistry2010 75 (3), 988-991Diastereoselective Diels−Alder Reactions with an Allenyl-Containing Spiro-Amido Chiral Auxiliary
Jeff R. Henderson, Julian P. Chesterman, Masood Parvez and Brian A. KeayThe Journal of Organic Chemistry2010 75 (3), 988-991A novel allenyl-containing 1,3-spiro-amido alcohol auxiliary has been prepared and used in a variety of diastereoselective Diels−Alder reactions providing exclusively endo adducts with diastereomeric ratios ranging from 2:1 to >99:1.
Total Synthesis of (−)-Cylindrocyclophanes A and F Exploiting the Reversible Nature of the Olefin Cross Metathesis Reaction
Amos B. Smith, III, Christopher M. Adams, Sergey A. Kozmin, and Daniel V. PaoneJournal of the American Chemical Society2001 123 (25), 5925-5937Total Synthesis of (−)-Cylindrocyclophanes A and F Exploiting the Reversible Nature of the Olefin Cross Metathesis Reaction
Amos B. Smith, III, Christopher M. Adams, Sergey A. Kozmin, and Daniel V. PaoneJournal of the American Chemical Society2001 123 (25), 5925-5937Efficient total syntheses of the C2-symmetric (−)-cylindrocyclophanes A and F (1a and 1f) have been achieved. The initial strategy featured the use of a common advanced intermediate to assemble in stepwise fashion the required macrocycle of 1f, exploiting ...
Total Synthesis of (−)-Ascochlorin via a Cyclobutenone-Based Benzannulation Strategy
Gregory B. Dudley, Katherine S. Takaki, Don D. Cha, and Rick L. DanheiserOrganic Letters2000 2 (21), 3407-3410Total Synthesis of (−)-Ascochlorin via a Cyclobutenone-Based Benzannulation Strategy
Gregory B. Dudley, Katherine S. Takaki, Don D. Cha, and Rick L. DanheiserOrganic Letters2000 2 (21), 3407-3410The application of a convergent benzannulation strategy in an efficient synthesis of (−)-ascochlorin is described.
Total Synthesis of (−)-Cylindrocyclophane F
Amos B. Smith, III, Sergey A. Kozmin, and Daniel V. PaoneJournal of the American Chemical Society1999 121 (32), 7423-7424Total Synthesis of (−)-Cylindrocyclophane F
Amos B. Smith, III, Sergey A. Kozmin, and Daniel V. PaoneJournal of the American Chemical Society1999 121 (32), 7423-7424
Full Text HTMLTools
-
Add to Favorites
-
Download Citation
-
Email a Colleague -
Permalink
Order Reprints
Rights & Permissions
Citation Alerts
History
- Published In Issue August, 1994
ACS
Network
Facebook
Tweet This
CiteULike
Newsvine
Digg This
Delicious
