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Roush, William R., Koyama, Kazuo, Curtin, Michael L., Moriarty, Kevin J. (1996) Studies on the Synthesis of Nargenicin A1:  Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels−Alder Reaction of an 18-Membered Macrolide. Journal Of The American Chemical Society, 118 (32) 7502-7512 doi:10.1021/ja9607796

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Reference TypeJournal (article/letter/editorial)
TitleStudies on the Synthesis of Nargenicin A1:  Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels−Alder Reaction of an 18-Membered Macrolide
JournalJournal Of The American Chemical Society
AuthorsRoush, William R.Author
Koyama, KazuoAuthor
Curtin, Michael L.Author
Moriarty, Kevin J.Author
Year1996 (January)Volume118
Issue32
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja9607796Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1505246Long-form Identifiermindat:1:5:1505246:3
GUID0
Full ReferenceRoush, William R., Koyama, Kazuo, Curtin, Michael L., Moriarty, Kevin J. (1996) Studies on the Synthesis of Nargenicin A1:  Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels−Alder Reaction of an 18-Membered Macrolide. Journal Of The American Chemical Society, 118 (32) 7502-7512 doi:10.1021/ja9607796
Plain TextRoush, William R., Koyama, Kazuo, Curtin, Michael L., Moriarty, Kevin J. (1996) Studies on the Synthesis of Nargenicin A1:  Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels−Alder Reaction of an 18-Membered Macrolide. Journal Of The American Chemical Society, 118 (32) 7502-7512 doi:10.1021/ja9607796
In(1996, January) Journal Of The American Chemical Society Vol. 118 (32) American Chemical Society (ACS)

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Roush, William R., Lin, Xiao-Fa (1995) Studies on the Synthesis of Aureolic Acid Antibiotics: Highly Stereoselective Synthesis of Aryl 2-Deoxy-.beta.-glycosides via the Mitsunobu Reaction and Synthesis of the Olivomycin A-B Disaccharide. Journal Of The American Chemical Society, 117 (8) 2236-2250 doi:10.1021/ja00113a013
Roush, William R., Sciotti, Richard J. (1998) Enantioselective Total Synthesis of (−)-Chlorothricolide via the Tandem Inter- and Intramolecular Diels−Alder Reaction of a Hexaenoate Intermediate. Journal Of The American Chemical Society, 120 (30) 7411-7419 doi:10.1021/ja980611f
Phoenix, Serge, Reddy, Maddi Sridhar, Deslongchamps, Pierre (2008) Total Synthesis of (+)-Cassaine via Transannular Diels−Alder Reaction. Journal Of The American Chemical Society, 130 (42) 13989-13995 doi:10.1021/ja805097s
Qi, Jun, Roush, William R. (2006) Synthesis of Precursors of the Agalacto (Exo) Fragment of the Quartromicins via an Auxiliary-Controlled Exo-Selective Diels−Alder Reaction. Organic Letters, 8. 2795-2798 doi:10.1021/ol0609208
Roush, William R., Hall, Steven E. (1981) Studies on the total synthesis of chlorothricolide: stereochemical aspects of the intramolecular Diels-Alder reactions of methyl undeca-2,8,10-trienoates. Journal Of The American Chemical Society, 103 (17) 5200-5211 doi:10.1021/ja00407a042
Dauben, William G., Kessel, Carl R., Takemura, Kazuo H. (1980) Simple, efficient total synthesis of cantharidin via a high-pressure Diels-Alder reaction. Journal Of The American Chemical Society, 102 (22) 6893-6894 doi:10.1021/ja00542a060
Roush, William R., Palkowitz, Alan D. (1987) Application of tartrate ester modified allylic boronates in organic synthesis: an efficient, highly stereoselective synthesis of the carbon(19)-carbon(29) segment of rifamycin S. Journal Of The American Chemical Society, 109 (3) 953-955 doi:10.1021/ja00237a082
Hunt, J. A., Roush, William R. (1996) Solid-Phase Synthesis of 6-Deoxyoligosaccharides. Journal Of The American Chemical Society, 118 (41) 9998-9999 doi:10.1021/ja962128f
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Frank, Scott A, Works, Andrea B, Roush, William R (2000) Studies on the synthesis of the decahydro-as-indacene ring system of (-)-spinosyn A via transannular Diels-Alder reactions of substituted (E,E,E)-cyclododeca-1,6,8-trienes. Canadian Journal of Chemistry, 78 (6). 757-771 doi:10.1139/v00-045
 
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