Asymmetric cis-Hydroxylation via Epoxydation-Carboxylation: A Formal Synthesis of (+)-Citreoviral

DOI: 10.1016/S0040-4039(00)95732-0

Source and publish data:

Tetrahedron Letters p. 375 - 378 (1987)

Update date:2022-08-04

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Authors:

Trost, Barry M.

Lynch, John K.

Angle, Steven R.

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Article abstract of DOI:10.1016/S0040-4039(00)95732-0

Asymmetric epoxydation of tiglyl alcohol combined with Pd(0) catalyzed conversion to the vicinal diol with retention of configuration provides an efficient asymmetric synthesis of a key intermediate to (+)-citreoviral and related compounds.

Full text of DOI:10.1016/S0040-4039(00)95732-0

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Article Doi

Asymmetric cis-Hydroxylation via Epoxydation-Carboxylation: A Formal Synthesis of (+)-Citreoviral

DOI: 10.1016/S0040-4039(00)95732-0

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)95732-0

Full text of DOI:10.1016/S0040-4039(00)95732-0

Products guided by the article

R&D Labs maybe for 110933-26-1

Relevant to this article

Auto-tandem catalysis: Synthesis of substituted 11H-indolo [3,2-c]quinolines via palladium-catalyzed intermolecular C-N and intramolecular C-C bond formation

Discovery of β-arrestin-biased β2-adrenoceptor agonists from 2-amino-2-phenylethanol derivatives

Catalytic enantioselective arylation of N-tosylarylimines with arylboronic acids using C2-symmetric cationic N-heterocyclic carbene Pd 2+ diaquo complexes

The divergent transformations of aromatic o-aminonitrile with carbonyl compound

An efficient synthesis of enantiomerically pure 2-[(2R)-arylmorpholin- 2-yl]ethanols, key intermediates of tachykinin receptor antagonist

Ruthenium complexes with tridentate PNX (X = O, S) donor ligands

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