STEREOSELECTIVE APPROACH TO TRISUBSTITUTED TETRAHYDROFURANS

DOI: 10.1016/S0040-4039(00)73723-3

Source and publish data:

Tetrahedron Letters p. 6251 - 6254 (1993)

Update date:2022-08-04

Topics:: Authors:

Mohr, Peter

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Article abstract of DOI:10.1016/S0040-4039(00)73723-3

Functionalized allylsilanes 1 undergo with acetals 2 under mild Broensted acid catalysis a transacetalization-ring closure reaction to afford in fair to good yield and high diastereoselectivity all-cis-tetrahydrofurans 3.The stereochemical outcome is inde

Full text of DOI:10.1016/S0040-4039(00)73723-3

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Article Doi

STEREOSELECTIVE APPROACH TO TRISUBSTITUTED TETRAHYDROFURANS

DOI: 10.1016/S0040-4039(00)73723-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)73723-3

Full text of DOI:10.1016/S0040-4039(00)73723-3

Products guided by the article

R&D Labs maybe for 153797-33-2

Relevant to this article

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Synthesis of functionalized polycyclic aromatic compounds via a formal [2 + 2]-cycloaddition

Solid-phase synthesis of peptide thioureas and thiazole-containing macrocycles through ru-catalyzed ring-closing metathesis

First total synthesis of the marine steroid alkaloid plakinamine B

Syntheses of 3H-labeled, 14C-labeled, and 2H4-labeled SCH 444877, phosphodiesterase type 5 inhibitors

4-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)- N -(4-methoxypyridin-2-yl) piperazine-1-carbothioamide (ML267), a potent inhibitor of bacterial phosphopantetheinyl transferase that attenuates secondary metabolism and thwarts bacterial growth

Syntheses of ³H-labeled, ¹⁴C-labeled, and ²H₄-labeled SCH 444877, phosphodiesterase type 5 inhibitors