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Utsumi, Naoto, Imai, Masanori, Tanaka, Fujie, Ramasastry, S. S. V., Barbas, Carlos F. (2007) Mimicking Aldolases through Organocatalysis: syn-Selective Aldol Reactions with Protected Dihydroxyacetone. Organic Letters, 9. 3445-3448 doi:10.1021/ol701467s

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Reference TypeJournal (article/letter/editorial)
TitleMimicking Aldolases through Organocatalysis: syn-Selective Aldol Reactions with Protected Dihydroxyacetone
JournalOrganic Letters
AuthorsUtsumi, NaotoAuthor
Imai, MasanoriAuthor
Tanaka, FujieAuthor
Ramasastry, S. S. V.Author
Barbas, Carlos F.Author
Year2007 (August)Volume9
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ol701467sSearch in ResearchGate
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Mindat Ref. ID10880219Long-form Identifiermindat:1:5:10880219:7
GUID0
Full ReferenceUtsumi, Naoto, Imai, Masanori, Tanaka, Fujie, Ramasastry, S. S. V., Barbas, Carlos F. (2007) Mimicking Aldolases through Organocatalysis: syn-Selective Aldol Reactions with Protected Dihydroxyacetone. Organic Letters, 9. 3445-3448 doi:10.1021/ol701467s
Plain TextUtsumi, Naoto, Imai, Masanori, Tanaka, Fujie, Ramasastry, S. S. V., Barbas, Carlos F. (2007) Mimicking Aldolases through Organocatalysis: syn-Selective Aldol Reactions with Protected Dihydroxyacetone. Organic Letters, 9. 3445-3448 doi:10.1021/ol701467s
In(n.d.) Organic Letters Vol. 9. American Chemical Society (ACS)

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Ramasastry, S. S. V., Albertshofer, Klaus, Utsumi, Naoto, Tanaka, Fujie, Barbas, Carlos F. (2007) Mimicking Fructose and Rhamnulose Aldolases: Organocatalyticsyn-Aldol Reactions with Unprotected Dihydroxyacetone. Angewandte Chemie, 119 (29). 5668-5671 doi:10.1002/ange.200701269
Ramasastry, S. S. V., Albertshofer, Klaus, Utsumi, Naoto, Tanaka, Fujie, Barbas, Carlos F. (2007) Mimicking Fructose and Rhamnulose Aldolases: Organocatalyticsyn-Aldol Reactions with Unprotected Dihydroxyacetone. Angewandte Chemie International Edition, 46 (29). 5572-5575 doi:10.1002/anie.200701269
Ramasastry, S. S. V., Albertshofer, Klaus, Utsumi, Naoto, Barbas, Carlos F. (2008) Water-Compatible Organocatalysts for Direct Asymmetricsyn-Aldol Reactions of Dihydroxyacetone and Aldehydes. Organic Letters, 10. 1621-1624 doi:10.1021/ol8002833
Ramasastry, S. S. V., Zhang, Haile, Tanaka, Fujie, Barbas, Carlos F. (2007) Direct Catalytic Asymmetric Synthesis ofanti-1,2-Amino Alcohols andsyn-1,2-Diols through Organocatalyticanti-Mannich andsyn-Aldol Reactions. Journal Of The American Chemical Society, 129 (2) 288-289 doi:10.1021/ja0677012
Suri, Jeff T., Ramachary, Dhevalapally B., Barbas, Carlos F. (2005) Mimicking Dihydroxy Acetone Phosphate-Utilizing Aldolases through Organocatalysis:  A Facile Route to Carbohydrates and Aminosugars†. Organic Letters, 7. 1383-1385 doi:10.1021/ol0502533
Utsumi, Naoto, Zhang, Haile, Tanaka, Fujie, Barbas, Carlos F. (2007) A Way to Highly Enantiomerically Enriched aza-Morita–Baylis–Hillman–Type Products. Angewandte Chemie, 119 (11). 1910-1912 doi:10.1002/ange.200603973
Utsumi, Naoto, Kitagaki, Shinji, Barbas, III, Carlos F. (2008) Organocatalytic Mannich-Type Reactions of Trifluoroethyl Thioesters. Organic Letters, 10. 3405-3408 doi:10.1021/ol801207x
Utsumi, Naoto, Zhang, Haile, Tanaka, Fujie, Barbas, Carlos F. (2007) A Way to Highly Enantiomerically Enriched aza-Morita–Baylis–Hillman–Type Products. Angewandte Chemie International Edition, 46 (11). 1878-1880 doi:10.1002/anie.200603973
Thayumanavan, Rajeswari, Tanaka, Fujie, Barbas, Carlos F. (2004) Direct Organocatalytic Asymmetric Aldol Reactions of α-Amino Aldehydes:  Expedient Syntheses of Highly Enantiomerically Enrichedanti-β-Hydroxy-α-amino Acids. Organic Letters, 6. 3541-3544 doi:10.1021/ol0485417
Mase, Nobuyuki, Tanaka, Fujie, Barbas, Carlos F. (2003) Rapid Fluorescent Screening for Bifunctional Amine−Acid Catalysts:  Efficient Syntheses of Quaternary Carbon-Containing Aldols under Organocatalysis. Organic Letters, 5. 4369-4372 doi:10.1021/ol035651p
Zhang, Haile, Mitsumori, Susumu, Utsumi, Naoto, Imai, Masanori, Garcia-Delgado, Noemi, Mifsud, Maria, Albertshofer, Klaus, Cheong, Paul Ha-Yeon, Houk, K. N., Tanaka, Fujie, Barbas, Carlos F. (2008) Catalysis of 3-Pyrrolidinecarboxylic Acid and Related Pyrrolidine Derivatives in Enantioselectiveanti-Mannich-Type Reactions:  Importance of the 3-Acid Group on Pyrrolidine for Stereocontrol. Journal Of The American Chemical Society, 130 (3) 875-886 doi:10.1021/ja074907+
 
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