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Orthogonal chemical functional groups

Introduction of Orthogonal Chemical Functional Groups into ManNAc... [Pg.2133]

The careful selection of the reactive building blocks ( reactophores ) is a key issue as they predetermine the core stmcture and the appended functional groups. Orthogonally protected functional groups minimise the number of chemical transformations on the solid support and thus will increase the overall yield. [Pg.130]

A diastereoselective ewrfo-cyclization into an oxidatively generated oxocarbenium ion was a key step in a formal synthesis of leucascandrolide A. Exposing 56 to CAN provided cw-tetrahydropyran 57 in high yield and with excellent stereocontrol (Scheme 3.20). This transformation provides further evidence that oxidative electrophile formation is tolerant of several functional groups and can be applied to complex molecule synthesis. The synthetic sequence also utilized a Lewis acid mediated ionization reaction to form an oxocarbenium ion in the presence of the homobenzylic ether (58, 59), illustrating that two carbocation precursors that ionize through chemically orthogonal conditions can be incorporated into the same structure. [Pg.57]

These considerations form the basis for the numerous techniques that are now available for the chemical modification of proteins. The sections that follow will examine these techniques and the reactive principles by which they function. A section describing reactions that display orthogonal reactivity to native protein functional groups has also been included because of the growing importance of these reactions as tools to label proteins in complex mixtures. Because it is not practical to summarize all protein bioconjugation methods here, this information instead is intended to serve as an introduction to the concepts that drive the development of these reactions. Several additional reviews and books on protein modification have been listed in the Further Reading section. [Pg.1609]

The if functions are not orthogonal in the group space since they do not transform like reps of the group. They are a convenient set, however, in problems of chemical valence. [Pg.133]


See other pages where Orthogonal chemical functional groups is mentioned: [Pg.128]    [Pg.128]    [Pg.81]    [Pg.2156]    [Pg.2175]    [Pg.21]    [Pg.672]    [Pg.789]    [Pg.614]    [Pg.203]    [Pg.165]    [Pg.8]    [Pg.9]    [Pg.61]    [Pg.160]    [Pg.193]    [Pg.328]    [Pg.247]    [Pg.26]    [Pg.432]    [Pg.236]    [Pg.208]    [Pg.144]    [Pg.6]    [Pg.26]    [Pg.29]    [Pg.44]    [Pg.37]    [Pg.1715]    [Pg.295]    [Pg.1015]    [Pg.2156]    [Pg.633]    [Pg.311]    [Pg.271]    [Pg.616]    [Pg.616]    [Pg.143]    [Pg.19]    [Pg.22]    [Pg.37]    [Pg.150]    [Pg.221]    [Pg.1078]    [Pg.89]   
See also in sourсe #XX -- [ Pg.2156 ]




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Chemical functionalization

Chemical functions

Chemical groups

Chemical groups functionalities

Chemicals functional

Functional groups, chemical

Orthogonal functions

Orthogonal groups

Orthogonally functionalized

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