Read More
Date: 13-9-2019
574
Date: 6-9-2019
543
Date: 27-10-2019
1033
|
Hydrogenolysis of Thioacetals
In contrast to the previous two procedures, this method of carbonyl deoxygenation requires two separate steps. It does, however, avoid treatment with strong base or acid. The first step is to convert the aldehyde or ketone into a thioacetal, as described earlier. These derivatives may be isolated and purified before continuing the reduction. The second step involves refluxing an acetone solution of the thioacetal over a reactive nickel catalyst, called Raney Nickel. All carbon-sulfur bonds undergo hydrogenolysis (the C–S bonds are broken by addition of hydrogen). In the following example, 1,2-ethanedithiol is used for preparing the thioacetal intermediate, because of the high yield this reactant usually affords. The bicyclic compound shown here has two carbonyl groups, one of which is sterically hindered (circled in orange). Consequently, a mono-thioacetal is easily prepared from the less-hindered ketone, and this is reduced without changing the remaining carbonyl function.
|
|
حمية العقل.. نظام صحي لإطالة شباب دماغك
|
|
|
|
|
إيرباص تكشف عن نموذج تجريبي من نصف طائرة ونصف هليكوبتر
|
|
|
|
شعبة مدارس الكفيل النسوية تطلق فعّاليات مخيم (بنات العقيدة) العشرين
|
|
قسم التربية والتعليم يعقد اجتماعاً تحضيرياً لملاكاته استعداداً لانطلاق برنامجه التأهيلي
|
|
متحف الكفيل يعقد أولى اجتماعاته التحضيرية لمؤتمره الدوليّ الخامس
|
|
وفد قسم الشؤون الفكرية وسفير العراق في فرنسا يبحثان سبل تعزيز التعاون المشترك
|