Big Chemical Encyclopedia

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

Articles Figures Tables About

Asymmetric ring-closing metathesis ARCM

Asymmetric microbial acyloin condensation, 16 402 Asymmetric oxidation, 23 735 Asymmetric ring-closing metathesis (ARCM), 26 922... [Pg.76]

Finally, there is a report on Mo-catalysed asymmetric ring closing metathesis (ARCM) for the enantioselective desymmetrisation of prochiral phosphinates and phosphine oxides (Scheme 6.53). This constitutes the first example where ARCM is used to prepare chiral compounds with a heteroatom as stereogenic centre. [Pg.343]

On the basis of the original studies [111-113], the DoM-cross-coupHng sequence represents a significant entry into chiral binaphthol (BINOL) and achiral biphenol (BIPOL) ligands (Table 14.18) [111-119], which are outside the scope of this review but are widely used for enantioselective reactions, for example, Et2Zn addition to aromatic aldehydes, the Mannich-type reactions, and the Diels-Alder as well as asymmetric ring-closing metathesis (ARCM) reactions. [Pg.1095]

See other pages where Asymmetric ring-closing metathesis ARCM is mentioned: [Pg.552]    [Pg.3]    [Pg.13]    [Pg.64]    [Pg.231]    [Pg.704]    [Pg.705]    [Pg.552]    [Pg.3]    [Pg.13]    [Pg.64]    [Pg.231]    [Pg.704]    [Pg.705]    [Pg.346]    [Pg.106]    [Pg.220]    [Pg.5611]    [Pg.5610]    [Pg.476]   
See also in sourсe #XX -- [ Pg.365 , Pg.366 ]



SEARCH



ARCM

ARCM (asymmetric ring closing

Asymmetric Ring-Closing Metathesis

Ring asymmetric

Ring metathesis

Ring-closed

Ring-closing

Ring-closing metatheses

Ring-closing metathesi

© 2024 chempedia.info