Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Route d

Address Angle route d El Jadida et Blvd. De la Grande... [Pg.194]

Other possible cyclizations may involve 5-epoxy alcohols such as the generic compound 2. In this case, two pathways are theoretically possible a more favored 6-exo cydization mode (Route c) giving rise to a THP ring, or an alternative 7-endo cydization mode providing an oxepane ring (Route d) (Eq. b, Scheme 8.1) [7]. [Pg.272]

Route d is a hydrogenation of thiirene dioxides. Since the preparation of thiirene dioxides is rather laborious, and many of them are prepared from the corresponding thiirane oxides6, this method has practically no preparative value, and the only example reported is the reduction of 18a to cis- 17d in a very low yield (8%)21. [Pg.414]

The mechanism of the polymerization contains ionic intermediate steps. The free H+ goes to a carbenium ion and, as shown in route B, rearranges to form tetrapropylene. It is highly likely that this actual tetrapropylene exists only in very small concentrations. The product variety is explained by the rearrangement of the carbenium ion to dodecene isomers according to route C. In addition, short-chain olefins formed by fragmentation (route D). Polymerization proceeds at almost 100% to mono olefins. Aromatics, paraffins, and diolefins exist only in trace amounts. The propylene tetramer is best characterized by its distillation range. [Pg.65]

A striking result of this reinvestigation (128, 129) is the observation that the ratio of the product ketone to the acetylene formed from a-bromo-p-aminostyrene is a function of the pH (Table Vll) but that the rate at which they are formed is not. As the pH increases from 3.9 to 13.1, the relative yield of acetylene increases from 16% to 85%. Therefore, the acetylene formation by elimination of a proton from the vinyl cation (path b in route D in Scheme XI) is more susceptible to an increase in base strength than is ketone formation via the enol (path a). This observation is a rare case of pH control over product composition in a 1-El reaction. [Pg.260]

In the case of terminal alkynes having oxygenated functions in the linear chain (Scheme 10, route D), Martin, Padron, and coworkers found that homopropargylic alcohols reacted properly, yielding 2-substituted dihydropyrans as sole products, probably via a Prins-type cyclization. This cyclization provides a new approach toward 2-alkyM-halo-5,6-dihydro-2//-pyrans through a concomitant C-C and C-O bond formation (Scheme 21) [35]. [Pg.16]

Figure 9. CO exposure experienced on escape route (D-D) numbers are probability of incapacitation (E-E) CO exposure of incapacitated person 5 meters from corridor exit. Numbers are probability of death. Line at 1778 ppm below which CO makes no contribution to death. Figure 9. CO exposure experienced on escape route (D-D) numbers are probability of incapacitation (E-E) CO exposure of incapacitated person 5 meters from corridor exit. Numbers are probability of death. Line at 1778 ppm below which CO makes no contribution to death.
The four hitherto known routes of the C-H insertion are shown in Scheme 1. In general, the insertion by singlet carbenes proceeds via route a in one step, whereas the reaction by triplet carbenes proceeds sequentially via route b, i.e., hydrogen abstraction followed by recombination of the radical pairs.4 Other stepwise mechanisms are hydride abstraction (route c) and proton abstraction (route d), both being followed by the recombination of ion pairs. However, extended study on routes c and d for synthetic purposes had not been done before we started, except for a few earlier studies on carbanion-promoted P C-H insertion reactions.5,6 Recent advances in transition metal-catalyzed... [Pg.288]

Waterborne transport Only port hinterland transport (Rotterdam) B - Port capacity and congestion hinterland routes D v... [Pg.579]

Vasanthan and Bhatty (1995) reported the use of pin milling and air classification as a technique for preconcentrating starch prior to wet isolation (Fig. E2.1.1, route D). Air classi-... [Pg.675]

There may be situations where it is too difficult to compute the free energy for a reaction or transformation along, for example, route D, whereas it may be relatively easy to compute the free energies for the three routes A, B, and C. Rearranging Eq. (11) gives... [Pg.375]

Fig. 3. Graphs of linear catalytic reaction mechanisms, (a), (b), (c), One-route (d), (e) two-route (f) multi-route mechanisms. Fig. 3. Graphs of linear catalytic reaction mechanisms, (a), (b), (c), One-route (d), (e) two-route (f) multi-route mechanisms.
Gosden JR, Middleton PG. Rout D Localization of the human oestrogen receptor gene to chromosome 6q24-Q27 by in situ hybridization. Cytogenet Cell Genet 1986 43(3-4) 218-220. [Pg.96]


See other pages where Route d is mentioned: [Pg.85]    [Pg.397]    [Pg.156]    [Pg.282]    [Pg.132]    [Pg.133]    [Pg.133]    [Pg.258]    [Pg.868]    [Pg.132]    [Pg.133]    [Pg.23]    [Pg.397]    [Pg.398]    [Pg.325]    [Pg.78]    [Pg.198]    [Pg.35]    [Pg.112]    [Pg.31]    [Pg.148]    [Pg.155]    [Pg.421]    [Pg.421]    [Pg.103]    [Pg.124]    [Pg.624]    [Pg.85]    [Pg.98]    [Pg.100]    [Pg.156]    [Pg.339]    [Pg.85]    [Pg.673]    [Pg.397]    [Pg.303]   


SEARCH



D Global Routing

Routes A-D with Respect to Mass Consumption, Environmental, Health and Safety Aspects

© 2024 chempedia.info