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OverviewDuring the past decade there has been a great increase in the use of protective groups, especially in the synthesis of large and complex organic molecules. Perhaps the greatest activity has been in the peptide field where such triumphs as the total synthesis of insulin and of bovine ribonuclease (molecular weight 13,700) have been achieved. Correspondingly, more protective groups have been devised for the protection of amino and imino groups than for any other functional group. There are many reviews and books on the synthesis of pep tides but there has been no general survey of protective groups since my 1 own review in 1963. At that time the five main methods for the removal of protective groups involved acid or base hydroly sis, reduction, oxidation, or thermal elimination reactions. Recent advances include the use of photo-sensitive and metal ion sensitive protective groups, and the attachment of functional groups to reactive polymers as a method of protec tion during the solid-phase synthesis of peptides and poly nucleotides. Another interesting development is the design and use of protective groups with a built-in 'safety-catch', which can be 'released' by a specific chemical reaction, so that an otherwise stable bond is made labile at the appropriate moment thereby allowing the protective group to be removed under very 2 mild conditions. My own interest in protective groups dates from 1944 when, as a student, I gave two lectures on the subject and produced an 11 page review including 70 references. Full Product DetailsAuthor: J. McOmiePublisher: Springer-Verlag New York Inc. Imprint: Springer-Verlag New York Inc. Edition: Softcover reprint of the original 1st ed. 1973 Dimensions: Width: 15.20cm , Height: 2.20cm , Length: 22.90cm Weight: 0.629kg ISBN: 9781468472202ISBN 10: 1468472208 Pages: 418 Publication Date: 26 November 2012 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: Manufactured on demand ![]() We will order this item for you from a manufactured on demand supplier. Table of Contents1 Protection of C-H Bonds.- 2 Protection of N-H Bonds and NR3.- 3 Protection of Alcholic Hydroxyl Groups and Glycols Systems.- 4 Protection of Phenols and Catechols.- 5 Protection of Carboxyl Groups.- 6 Protection of Phosphoric and Related Acids.- 7 Protection of Thiols.- 8 Protection of Carbon-Carbon Multiple Bonds.- 9 Protection of Aldehydes and Ketones.- 10 Protection of Miscellaneous Groups.ReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |