Photochemistry of phthalimides: decarboxylation, addition, macrocyclization and deprotection

Oelgemöller, Michael, and Griesbeck, A.G. (2000) Photochemistry of phthalimides: decarboxylation, addition, macrocyclization and deprotection. In: Proceedings of the Internet Photochemistry and Photobiology Conference (3), pp. 1-9. From: Third Internet Photochemistry and Photobiology Conference, 24 November - 24 December 2000, Online.

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Abstract

A large number of useful photochemical transformations in the phthalimide series were developed. These processes allow the photochemical synthesis of interesting new compounds via addition, ring expansion, cyclization or fragmentation reactions. Beside the spacer fragments shown in here also peptide or olefinic linkers were examined, and next to phthalimides other imides like quinolinic- and trimellitic acid imides were suitable chromophores for PET-reactions.

Item ID: 54686
Item Type: Conference Item (Non-Refereed Research Paper)
Keywords: photochemistry; photodecarboxylation; phthalimides; photoinduced electron transfer
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Date Deposited: 24 Jul 2018 00:05
FoR Codes: 03 CHEMICAL SCIENCES > 0305 Organic Chemistry > 030503 Organic Chemical Synthesis @ 40%
03 CHEMICAL SCIENCES > 0305 Organic Chemistry > 030505 Physical Organic Chemistry @ 30%
03 CHEMICAL SCIENCES > 0305 Organic Chemistry > 030501 Free Radical Chemistry @ 30%
SEO Codes: 97 EXPANDING KNOWLEDGE > 970103 Expanding Knowledge in the Chemical Sciences @ 100%
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