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Selective catalytic hydrogenation of the trans, trans isomer from a mixture of 2,4-hexadienes.

✍ Scribed by Gérard Platbrood; Liliane Wilputte-Steinert


Publisher
Elsevier Science
Year
1974
Tongue
French
Weight
107 KB
Volume
15
Category
Article
ISSN
0040-4039

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✦ Synopsis


SELECTIVE CATALYTIC HYDROGENATION OF THE TRANS, TRANS ISOMER FROM

A MIXTURE OF 2,4-HEXADIENES.


📜 SIMILAR VOLUMES


Photochemistry of a 2,3-benzo-2,4-cycloo
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## Evidence that the highly reactive trans,cis-2,4-cyclooctadienone x is an intermediate in -- the photoreactions of the cis cis isomer has been presented.' \_\*---The trans ketone < was stable at dimers or trapping products

Synthesis of a trans-benzo-[f]-heterodec
✍ Martin Studer; Peter Baumeister; Hans-Ulrich Blaser; Joe Bach 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 970 KB

Racemic trans-1A ( translo-metboxy-1,3,4,%,5,1Ob-hexahydro-2H-[ 11 benzopyrano [ 3,4-b] pyridine, see Scheme 1) was obtained in high chemical yield (up to 89%) and with excellent stereoselectivity (95% truns) by catalytic hydrogenationdehalogenation of 7-chloro-lo-methoxy-3,4,4a,Stetrahydro-2H-[ 1 ]