Total Synthesis of the Cytotoxic Threo, Trans, Erythro, Cis, Threo Annonaceous Acetogenin Trilobin-Reference-Cited by-同舟云学术

Total Synthesis of the Cytotoxic Threo, Trans, Erythro, Cis, Threo Annonaceous Acetogenin Trilobin

Published:1999-01-15 Issue:3 Volume:64 Page:971-975
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Marshall James A.¹,Jiang Hongjian¹

Affiliation:

1. Department of Chemistry University of Virginia, Charlottesville, Virginia 22901

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982057y

Reference21 articles.

1. The absolute configuration of trilobacin and trilobin, a novel highly potent acetogenin from the stem bark of Asimina triloba (Annonaceae)

2. (b) Reviews: Cavé, A.; Figadére, B.; Laureno, A.; Cortes, D. InProgressintheChemistryofNaturalProducts; Herz, W., Kirby, G.W., Moore, R. E., Steglich, W., Tamm, Ch., Eds.; Springer: New York, 1997; Vol. 70, pp 81−288. Zeng, L.; Ye, Q.; Oberlies, N. H.; Shi, G.; Gu, Z.M.; He, K.; McLaughlin, J. L.Nat.Prod.Rep.1996, 275.

3. Highly Efficient Synthesis of the Potent Antitumor Annonaceous Acetogenin (+)-Parviflorin

4. An Efficient Bidirectional Approach to the C2-Symmetric Stereoisomers of the Bistetrahydrofuran Core of the Acetogenins

5. Total Synthesis of the Annonaceous Acetogenin (+)-Asimicin. Development of a New Bidirectional Strategy

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