Stereoselective partial hydrogenation of the triple bond in methyl 2-ethyl-6,6-dimethylhept-2-en-4-ynoate: A comparison of lindlar and montmorillonite catalysts-Reference-Cited by-同舟云学术

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Stereoselective partial hydrogenation of the triple bond in methyl 2-ethyl-6,6-dimethylhept-2-en-4-ynoate: A comparison of lindlar and montmorillonite catalysts

Published:1990-01 Issue:5 Volume:46 Page:1569-1578
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Nikles Martin,Bur Daniel,Séquin Urs

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Concerning the reactivity of 1,2:3,4-diepoxides towards nucleophiles

2. Ein hochselektiver Montmorillonit-Katalysator zur Hydrierung von Alkinen, Alkeninen und Alkadienen

3. Herstellung von 2-Alkynalen und 1-Alkynyl-ketonen aus Lithium-acetyleniden und Carbonsäure-estern

4. Facile synthesis of tert-butylacetylene

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2. Synthesis of Conjugated Dienes and Polyenes;PATAI'S Chemistry of Functional Groups;2009-12-15

3. 2 Hydrogen-NMR. Coupling constant. Substance no. 1577ff;Landolt-Börnstein - Group III Condensed Matter;2000

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5. 2 Hydrogen-1 NMR. References;Landolt-Börnstein - Group III Condensed Matter;2000

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