Macrocycle Formation by Ring-Closing-Metathesis. 2. An Efficient Synthesis of 
Enantiomerically Pure (R)-(+)-Lasiodiplodin

Fürstner, Alois; Kindler, Nicole

doi:10.1016/0040-4039(96)01590-0

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Macrocycle Formation by Ring-Closing-Metathesis. 2. An Efficient Synthesis of Enantiomerically Pure (R)-(+)-Lasiodiplodin

Fürstner, A., & Kindler, N. (1996). Macrocycle Formation by Ring-Closing-Metathesis. 2. An Efficient Synthesis of Enantiomerically Pure (R)-(+)-Lasiodiplodin. Tetrahedron Letters, 37(39), 7005-7008. doi:10.1016/0040-4039(96)01590-0.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0024-0798-E Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0024-0799-C

Genre: Journal Article

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Creators:
Fürstner, Alois¹, Author
Kindler, Nicole¹, Author

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1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584

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Abstract: A highly efficient and flexible route to the macrolide (R)-(+)-lasiodiplodin 1 and its de-Omethyl congener 2 is outlined, which is based on the formation of the 12-membered ring by ringclosing metathesis (RCM) as the key step.

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Language(s): eng - English

Dates: Date issued: 1996-09-23

Publication Status: Issued

Pages: 4

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Rev. Type: Peer

Identifiers: DOI: 10.1016/0040-4039(96)01590-0

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Title: Tetrahedron Letters

Other : Tetrahedron Lett.

Source Genre: Journal

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Publ. Info: Oxford : Pergamon

Pages: 4 Volume / Issue: 37 (39) Sequence Number: - Start / End Page: 7005 - 7008 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772