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  Stereoselective Synthesis of Dienyl-Carboxylate Building Blocks: Formal Synthesis of Inthomycin C

Souris, C., Frébault, F., Patel, A., Audisio, D., Houk, K. N., & Maulide, N. (2013). Stereoselective Synthesis of Dienyl-Carboxylate Building Blocks: Formal Synthesis of Inthomycin C. Organic Letters, 15(13), 3242-3245. doi:10.1021/ol401226y.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-A39A-6 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-001A-154E-8
Genre: Journal Article

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 Creators:
Souris, Caroline1, Author           
Frébault, Frédéric1, Author           
Patel, Ashay2, Author
Audisio, Davide1, Author           
Houk, K. N.2, Author
Maulide, Nuno1, Author           
Affiliations:
1Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445614              
2Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA, ou_persistent22              

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Free keywords: SMALL-MOLECULE SYNTHESIS; CYCLOBUTENE ELECTROCYCLIC REACTIONS; ASYMMETRIC ALLYLIC ALKYLATION; OXIDATION-WITTIG REACTIONS; CROSS-COUPLING REACTIONS; ORGANOBORON COMPOUNDS; VERSATILE; (+)-INTHOMYCIN-B; OXAZOLOMYCIN; COMPETITION
 Abstract: A direct synthesis of stereodefined halodienes is reported. Those key building blocks enable a concise access to polyenic products, as demonstrated in a modular synthesis of Inthomycin C.

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Language(s): eng - English
 Dates: 2013-06-132013-07-05
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ol401226y
 Degree: -

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Title: Organic Letters
  Other : Org. Lett.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 15 (13) Sequence Number: - Start / End Page: 3242 - 3245 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338