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Cyclization reactions 6- endo- trigonal

In summary, certain reactions with diterpenoid alkaloid imines proceeded by a disfavored 5-endo-trigonal process, whereas in other cases, such as the reactions with glycidol, a favored 6-endo-trigonal process was followed. The Baldwin rules should be modified to accomodate the exceptional behavior of the tertiary immonium salts. Recently, examples of similar reactions demonstrating the violation of the Baldwin cyclization rules have been reported (156-158). [Pg.159]

This reaction is useful for cyclizations involving 6-endo-trigonal (eq 14) and allowed 1-endo trigonal processes (eq 15), but not for those involving 5-endo trigonal processes (eq 16). These observations are consistent with the Baldwin rules. [Pg.379]

One typical radical reaction is cyclization. This cyclization has been used as an indirect proof for radical reactions and a strategic method for the construction of 5- and 6-membered cyclic compounds. The experienced rule for the cyclization is Baldwin s rule [19]. There are two cyclization modes, i.e. exo and endo moreover, there are three types of hybridization in a carbon atom, sp3 (tetrahedral tet), sp2 (trigonal trig), and sp (digonal dig). Baldwin s rule is the cyclization rule based on the experimentally obtained cyclization results. The cyclization mode and kinds of hybridization in an intramolecular radical acceptor are shown in Figure 1.15. [Pg.21]

Thus, it is called exo , when the cyclization occurs on the inside of the unsaturated carbon-carbon bond, and it is called endo , when the cyclization occurs on the outside of the unsaturated carbon-carbon bond. Moreover, it is tet (tetrahedral 109.5°), when the carbon-carbon bond at the reaction site is sp3 hybridization it is trig (trigonal, 120°), when the unsaturated carbon-carbon bond at the reaction site is sp2 hybridization and it is dig (digonal, 180°), when the unsaturated carbon-carbon bond at the reaction site is sp hybridization. For example, there are two types of cyclization manner in 5-hexen-l-yl radical, exo-trig and endo-trig, based on the above classification. Since a 5-membered cyclopentylmethyl radical is formed through exo-trig cyclization, it is finally... [Pg.21]

A paper on the application of Baldwin s rules (see Chapter 6) to specific heterocyclic examples has appeared, and more are anticipated in this potentially fruitful area. Compounds have been examined as substrates for disfavoured 5-Endo-Trigonalring forming reactions. Ketols (1) and (2) did not cyclize to the furanones (3) and (4) respectively, under basic conditions, but the reactions were smoothly achieved with acid catalysis a result best explained by the intermediacy of the enol (5) using the 5-Exo-Trigonal process (Scheme 1). Treatment of the unsaturated... [Pg.197]


See other pages where Cyclization reactions 6- endo- trigonal is mentioned: [Pg.310]    [Pg.37]    [Pg.1140]    [Pg.1140]    [Pg.1140]    [Pg.1140]    [Pg.810]    [Pg.124]    [Pg.198]    [Pg.274]   


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Cyclization reactions

Cyclizations 5- endo-trigonal

Cyclizations 5-endo

Endo-cyclization reactions

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