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Protective Groups in Organic Synthesis

T.W. Greene P.G.M. Wuts, Protective Groups in Organic Synthesis (2nd edition) J. Wiley Sons, 1991. [Pg.57]

T. W. Greene, Protective Groups in Organic Synthesis, ]ohxi Wiley Sons, Inc., New York, 1988, p. 114. [Pg.364]

Ethers are among the most used protective groups in organic synthesis. They vary from the simplest, most robust, methyl ether to the more elaborate, substituted, trityl ethers developed for use in nucleotide synthesis. They are formed and removed under a wide variety of conditions. Some of the ethers that have been used to protect alcohols are included in Reactivity Chart 1. ... [Pg.14]

Greene, T. W. Wuts, P. G. M. Protective Groups in Organic Synthesis, Second Edition, John Wiley Sons New York, 1991. [Pg.263]

M. Lalonde and T. H. Chan. Use of organosilicon reagents as protective groups in organic synthesis. Synthesis 817 (1985). [Pg.97]

Greene TW, Wuts PGM (1999) Protective groups in organic synthesis. Wiley, New York... [Pg.133]

J. F. W. McOmie, ed., Protective Groups in Organic Synthesis, Plenum Press New York, 1973. [Pg.1259]


See other pages where Protective Groups in Organic Synthesis is mentioned: [Pg.138]    [Pg.1]    [Pg.2]    [Pg.4]    [Pg.5]    [Pg.6]    [Pg.7]    [Pg.8]    [Pg.15]    [Pg.485]    [Pg.2]    [Pg.4]    [Pg.6]    [Pg.8]    [Pg.10]    [Pg.12]    [Pg.14]    [Pg.16]    [Pg.23]    [Pg.23]    [Pg.803]    [Pg.160]    [Pg.143]    [Pg.613]    [Pg.941]    [Pg.485]    [Pg.493]   
See also in sourсe #XX -- [ Pg.627 ]




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Protective Groups in Organic

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