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Griesbeck, Axel G., Mauder, Harald, Müller, Ingrid (1992) Photochemistry ofN-Phthaloyl α-Amino Acid Esters: A New Approach to β,γ-Unsaturated α-Amino Acid, Dihydrobenzazepinedione, and Pyrrolizidinone Derivatives. Chemische Berichte, 125. 2467-2475 doi:10.1002/cber.19921251119

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Reference TypeJournal (article/letter/editorial)
TitlePhotochemistry ofN-Phthaloyl α-Amino Acid Esters: A New Approach to β,γ-Unsaturated α-Amino Acid, Dihydrobenzazepinedione, and Pyrrolizidinone Derivatives
JournalChemische Berichte
AuthorsGriesbeck, Axel G.Author
Mauder, HaraldAuthor
Müller, IngridAuthor
Year1992 (November)Volume125
PublisherWiley
DOIdoi:10.1002/cber.19921251119Search in ResearchGate
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Mindat Ref. ID4332221Long-form Identifiermindat:1:5:4332221:3
GUID0
Full ReferenceGriesbeck, Axel G., Mauder, Harald, Müller, Ingrid (1992) Photochemistry ofN-Phthaloyl α-Amino Acid Esters: A New Approach to β,γ-Unsaturated α-Amino Acid, Dihydrobenzazepinedione, and Pyrrolizidinone Derivatives. Chemische Berichte, 125. 2467-2475 doi:10.1002/cber.19921251119
Plain TextGriesbeck, Axel G., Mauder, Harald, Müller, Ingrid (1992) Photochemistry ofN-Phthaloyl α-Amino Acid Esters: A New Approach to β,γ-Unsaturated α-Amino Acid, Dihydrobenzazepinedione, and Pyrrolizidinone Derivatives. Chemische Berichte, 125. 2467-2475 doi:10.1002/cber.19921251119
In(1992) Chemische Berichte Vol. 125. Wiley

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Griesbeck, Axel G., Mauder, Harald (1992) Photochemie vonN-Phthaloyl-α-aminosäureestern: Ein neuer Zugang zu β,γ-ungesättigten α-Aminosäuren und Dihydrobenzazepindionen. Angewandte Chemie, 104 (1). 97-99 doi:10.1002/ange.19921040134
Griesbeck, Axel G., Mauder, Harald, Peters, Karl, Peters, Eva-Maria, Schnering, Hans Georg Von (1991) Photocycloadditionen mit α- und β-Naphthaldehyd: Vollständige Umkehr der Diastereoselektivität als Konsequenz unterschiedlich konfigurierter elektronischer Zustände. Chemische Berichte, 124. 407-410 doi:10.1002/cber.19911240227
KOLASA, T. (1983) ChemInform Abstract: AN EFFECTIVE SYNTHESIS OF α,β-DEHYDRO-α-AMINO ACID DERIVATIVES FROM N-ACYL-N-HYDROXY-α-AMINO ACID ESTERS. Chemischer Informationsdienst, 14 (47) doi:10.1002/chin.198347121
BRTNIK, F., ZAORAL, M. (1977) ChemInform Abstract: AMINO ACIDS AND PEPTIDES. CXXXV. SYNTHESIS OF DERIVATIVES AND PEPTIDES OF α-AMINO-β-GUANIDINOPROPIONIC ACID AND α-AMINO-Γ-GUANIDINOBUTYRIC ACID. Chemischer Informationsdienst, 8 (4) doi:10.1002/chin.197704324
Ulbrich, Dirk, Daniliuc, Constantin G., Haufe, Günter (2016) Halofluorination of N-protected α,β-dehydro-α-amino acid esters—A convenient synthesis of α-fluoro-α-amino acid derivatives. Journal of Fluorine Chemistry, 188. 65-75 doi:10.1016/j.jfluchem.2016.06.006
Wada, Makoto, Sano, Takashi, Mitsunobu, Oyo (1973) Stereospecific and Stereoselective Reactions. II. Preparation of Esters ofN-Phthaloyl-α-amino Acid from Esters of α-Hydroxy Acid. Bulletin of the Chemical Society of Japan, 46 (9). 2833-2835 doi:10.1246/bcsj.46.2833
CHARI, R. V. J., WEMPLE, J. (1979) ChemInform Abstract: A SIMPLE, EFFICIENT SYNTHESIS OF β-METHYLENE PHENYLALANINE. A NEW APPROACH TO THE PREPARATION OF β,Γ-UNSATURATED α-AMINO ACID ENZYME SUBSTRATE ANALOGS. Chemischer Informationsdienst, 10 (19) doi:10.1002/chin.197919216
Brtník, F., Zaoral, M. (1976) Synthesis of derivatives and peptides of α-amino-β-guanidinopropionic acid and α-amino-γ-guanidinobutyric acid. Collection of Czechoslovak Chemical Communications, 41. 2969-2977 doi:10.1135/cccc19762969
Griesbeck, Axel G, Bondock, Samir (2003) Photo aldol reactions with 5-methoxyoxazoles: Highly regio- and diastereoselective synthesis of α-amino β-hydroxy carboxylic acid derivatives. Canadian Journal of Chemistry, 81 (6). 555-559 doi:10.1139/v03-029
SHIN, C., YONEZAWA, Y., YOSHIMURA, J. (1977) ChemInform Abstract: A GENERAL SYNTHESIS OF α,β-UNSATURATED α-AMINO ACID ETHYL ESTERS. Chemischer Informationsdienst, 8 (12) doi:10.1002/chin.197712150
Srikanth, G. S. C., Castle, Steven L. (2004) Synthesis of β-Substituted α-Amino Acids via Lewis Acid Promoted Radical Conjugate Additions to α,β-Unsaturated α-Nitro Esters and Amides. Organic Letters, 6. 449-452 doi:10.1021/ol036461h
 
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