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Degnan, Andrew P., Meyers, A. I. (1999) Total Syntheses of (−)-Herbertenediol, (−)-Mastigophorene A, and (−)-Mastigophorene B. Combined Utility of Chiral Bicyclic Lactams and Chiral Aryl Oxazolines. Journal Of The American Chemical Society, 121 (12) 2762-2769 doi:10.1021/ja984182x

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Reference TypeJournal (article/letter/editorial)
TitleTotal Syntheses of (−)-Herbertenediol, (−)-Mastigophorene A, and (−)-Mastigophorene B. Combined Utility of Chiral Bicyclic Lactams and Chiral Aryl Oxazolines
JournalJournal Of The American Chemical Society
AuthorsDegnan, Andrew P.Author
Meyers, A. I.Author
Year1999 (March)Volume121
Issue12
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja984182xSearch in ResearchGate
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Mindat Ref. ID1543022Long-form Identifiermindat:1:5:1543022:7
GUID0
Full ReferenceDegnan, Andrew P., Meyers, A. I. (1999) Total Syntheses of (−)-Herbertenediol, (−)-Mastigophorene A, and (−)-Mastigophorene B. Combined Utility of Chiral Bicyclic Lactams and Chiral Aryl Oxazolines. Journal Of The American Chemical Society, 121 (12) 2762-2769 doi:10.1021/ja984182x
Plain TextDegnan, Andrew P., Meyers, A. I. (1999) Total Syntheses of (−)-Herbertenediol, (−)-Mastigophorene A, and (−)-Mastigophorene B. Combined Utility of Chiral Bicyclic Lactams and Chiral Aryl Oxazolines. Journal Of The American Chemical Society, 121 (12) 2762-2769 doi:10.1021/ja984182x
In(1999, March) Journal Of The American Chemical Society Vol. 121 (12) American Chemical Society (ACS)

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Meyers, A. I., Lutomski, Kathryn A. (1982) Enantioselective synthesis of binaphthyls via nucleophilic aromatic substitution on chiral oxazolines. Journal Of The American Chemical Society, 104 (3) 879-881 doi:10.1021/ja00367a053
Meyers, A. I., Knaus, Gerald (1974) Oxazolines. XIV. Asymmetric synthesis of R and S dialkylacetic acids from a single chiral oxazoline. Journal Of The American Chemical Society, 96 (20) 6508-6510 doi:10.1021/ja00827a041
Meyers, A. I., Snyder, Evan S., Ackerman, Joseph J. H. (1978) Stereochemistry of metalation and alkylation of chiral oxazolines. A carbon-13 nuclear magnetic resonance study of lithio oxazolines. Journal Of The American Chemical Society, 100 (26) 8186-8189 doi:10.1021/ja00494a028
MEYERS, A. I., LEFKER, B. A. (1986) ChemInform Abstract: Chiral Bicyclic Lactams for Asymmetrie Synthesis of Quaternary Carbons. Chemischer Informationsdienst, 17 (49) doi:10.1002/chin.198649302
Meyers, A. I., Whitten, Charles E. (1975) Oxazolines. XIX. Asymmetric synthesis of 3-substituted alkanoic acids via conjugated addition of organolithium reagents to chiral oxazolines. Journal Of The American Chemical Society, 97 (21) 6266-6267 doi:10.1021/ja00854a065
Meyers, A. I., Knaus, Gerald, Kamata, K. (1974) Synthesis via 2-oxazolines. IV. Asymmetric synthesis of 2-methylalkanoic acids from a chiral oxazoline. Journal Of The American Chemical Society, 96 (1) 268-270 doi:10.1021/ja00808a054
Meyers, A. I., Knaus, Gerald, Kamata, Kazuyuki, Ford, Michael E. (1976) Asymmetric synthesis of R and S .alpha.-alkylalkanoic acids from metalation and alkylation of chiral 2-oxazolines. Journal Of The American Chemical Society, 98 (2) 567-576 doi:10.1021/ja00418a041
Meyers, A. I., Mihelich, Edward D. (1975) Oxazolines. XXII. Nucleophilic aromatic substitution on aryl oxazolines. Efficient approach to unsymmetrically substituted biphenyls and o-alkyl benzoic acids. Journal Of The American Chemical Society, 97 (25) 7383-7385 doi:10.1021/ja00858a034
Meyers, A. I., Flisak, Joseph R., Aitken, R. Alan (1987) Asymmetric synthesis of (-)-steganone. Further application of chiral biaryl syntheses. Journal Of The American Chemical Society, 109 (18) 5446-5452 doi:10.1021/ja00252a022
Hoobler, M. A., Bergbreiter, David E., Newcomb, Martin (1978) Origins of stereoselectivity in asymmetric syntheses using chiral oxazolines. Journal Of The American Chemical Society, 100 (26) 8182-8185 doi:10.1021/ja00494a027
Meyers, A. I., Kamata, K. (1976) Oxazolines. XXI. Kinetic resolution of sec-alkyl halides and simultaneous asymmetric synthesis of 3-alkylalkanoic acids using a chiral oxazoline. A method for determining absolute configurations and maximum optical rotations. Journal Of The American Chemical Society, 98 (8) 2290-2294 doi:10.1021/ja00424a049
 
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