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David Lawrence Gray - Publications

Affiliations: 
2003 Scripps Research Institute, La Jolla, La Jolla, CA, United States 
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12 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Nicolaou KC, Gray D. Total Synthesis of Hybocarpone We thank Dr. D. H. Huang, Dr. G. Siuzdak and Dr. I. Ioannou for NMR spectroscopic, mass spectrometric and computational assistance, respectively. Financial support for this work was provided by the Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Novartis, Pfizer, CaPCURE, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 761-763. PMID 11241615 DOI: 10.1002/1521-3773(20010216)40:4<761::Aid-Anie7610>3.0.Co;2-0  0.313
2004 Nicolaou KC, Gray DL, Tae J. Total synthesis of hamigerans and analogues thereof. Photochemical generation and Diels-Alder trapping of hydroxy-o-quinodimethanes. Journal of the American Chemical Society. 126: 613-27. PMID 14719961 DOI: 10.1021/Ja030498F  0.423
2004 Nicolaou KC, Gray DL. Total synthesis of hybocarpone and analogues thereof. A facile dimerization of naphthazarins to pentacyclic systems. Journal of the American Chemical Society. 126: 607-12. PMID 14719960 DOI: 10.1021/Ja030497N  0.4
2002 Nicolaou KC, Gray DL, Montagnon T, Harrison ST. Oxidation of silyl enol ethers by using IBX and IBX.N-oxide complexes: a mild and selective reaction for the synthesis of enones. Angewandte Chemie (International Ed. in English). 41: 996-1000. PMID 12491292 DOI: 10.1002/1521-3773(20020315)41:6<996::Aid-Anie996>3.0.Co;2-I  0.542
2001 Nicolaou KC, Gray D, Tae J. Total Synthesis of Hamigerans: Part 2. Implementation of the Intramolecular Diels-Alder Trapping of Photochemically Generated Hydroxy-o-quinodimethanes; Strategy and Completion of the Synthesis This work was financially supported by the National Institutes of Health (USA) and The Skaggs Institute for Chemical Biology, and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 3679-3683. PMID 11592220 DOI: 10.1002/1521-3773(20011001)40:19<3679::Aid-Anie3679>3.0.Co;2-T  0.41
2001 Nicolaou KC, Gray D, Tae J. Total Synthesis of Hamigerans: Part 1. Development of Synthetic Technology for the Construction of Benzannulated Polycyclic Systems by the Intramolecular Trapping of Photogenerated Hydroxy-o-quinodimethanes and Synthesis of Key Building Blocks This work was financially supported by the National Institutes of Health (USA) and The Skaggs Institute for Chemical Biology, and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 3675-3678. PMID 11592219 DOI: 10.1002/1521-3773(20011001)40:19<3675::Aid-Anie3675>3.0.Co;2-G  0.402
2001 Nicolaou KC, Gray D, Tae J. Total synthesis of hamigerans: Part 2. Implementation of the intramolecular Diels - Alder trapping of photochemically generated hydroxy-o-quinodimethanes; strategy and completion of the synthesis Angewandte Chemie - International Edition. 40: 3679-3683. DOI: 10.1002/1521-3773(20011001)40:19<3679::AID-ANIE3679>3.0.CO;2-T  0.425
2001 Nicolaou KC, Gray D, Tae J. Total synthesis of hamigerans: Part 1. Development of synthetic technology for the construction of benzannulated polycyclic systems by the intramolecular trapping of photogenerated hydroxy-o-quinodimethanes and synthesis of key building blocks Angewandte Chemie - International Edition. 40: 3675-3678. DOI: 10.1002/1521-3773(20011001)40:19<3675::AID-ANIE3675>3.0.CO;2-G  0.404
2001 Nicolaou KC, Gray D, Tae J. Totalsynthese der Hamigerane - Teil 2: Anwendung der intramolekularen Diels-Alder-Reaktion zum Abfangen photochemisch erzeugter Hydroxy-o-chinodimethane sowie Strategie und Abschluss der Synthese Angewandte Chemie. 113: 3791-3795. DOI: 10.1002/1521-3757(20011001)113:19<3791::Aid-Ange3791>3.0.Co;2-J  0.374
2001 Nicolaou KC, Gray D, Tae J. Totalsynthese der Hamigerane - Teil 1: Entwicklung einer Synthesemethode für den Aufbau benzanellierter polycyclischer Systeme durch intramolekulares Abfangen von photochemisch erzeugten Hydroxy-o-chinodimethanen und Synthese von Schlüsselintermediaten Angewandte Chemie. 113: 3787-3790. DOI: 10.1002/1521-3757(20011001)113:19<3787::Aid-Ange3787>3.0.Co;2-M  0.342
1999 Nicolaou KC, Xu J, Murphy F, Barluenga S, Baudoin O, Wei Hx, Gray DL, Ohshima T. Total Synthesis of Sanglifehrin A. Angewandte Chemie (International Ed. in English). 38: 2447-2451. PMID 10458817 DOI: 10.1002/(Sici)1521-3773(19990816)38:16<2447::Aid-Anie2447>3.0.Co;2-O  0.61
1999 Nicolaou K, Xu J, Murphy F, Barluenga S, Baudoin O, Wei H, Gray D, Ohshima T. Totalsynthese von Sanglifehrin A Angewandte Chemie. 111: 2599-2604. DOI: 10.1002/(Sici)1521-3757(19990816)111:16<2599::Aid-Ange2599>3.0.Co;2-7  0.576
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