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KECK, G. E., ABBOTT, D. E. (1984) ChemInform Abstract: STEREOCHEMICAL CONSEQUENCES FOR THE LEWIS ACID MEDIATED ADDITIONS OF ALLYL AND CROTYLTRI-N-BUTYLSTANNANE TO CHIRAL β-HYDROXY ALDEHYDE DERIVATIVES. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435111

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Reference TypeJournal (article/letter/editorial)
TitleChemInform Abstract: STEREOCHEMICAL CONSEQUENCES FOR THE LEWIS ACID MEDIATED ADDITIONS OF ALLYL AND CROTYLTRI-N-BUTYLSTANNANE TO CHIRAL β-HYDROXY ALDEHYDE DERIVATIVES
JournalChemischer Informationsdienst
AuthorsKECK, G. E.Author
ABBOTT, D. E.Author
Year1984 (August 28)Volume15
Issue35
PublisherWiley
DOIdoi:10.1002/chin.198435111Search in ResearchGate
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Mindat Ref. ID14892432Long-form Identifiermindat:1:5:14892432:3
GUID0
Full ReferenceKECK, G. E., ABBOTT, D. E. (1984) ChemInform Abstract: STEREOCHEMICAL CONSEQUENCES FOR THE LEWIS ACID MEDIATED ADDITIONS OF ALLYL AND CROTYLTRI-N-BUTYLSTANNANE TO CHIRAL β-HYDROXY ALDEHYDE DERIVATIVES. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435111
Plain TextKECK, G. E., ABBOTT, D. E. (1984) ChemInform Abstract: STEREOCHEMICAL CONSEQUENCES FOR THE LEWIS ACID MEDIATED ADDITIONS OF ALLYL AND CROTYLTRI-N-BUTYLSTANNANE TO CHIRAL β-HYDROXY ALDEHYDE DERIVATIVES. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435111
In(1984, August) Chemischer Informationsdienst Vol. 15 (35) Wiley

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KECK, G. E., BODEN, E. P. (1984) ChemInform Abstract: CHELATION CONTROLLED DIASTEREOFACIAL SELECTIVITY IN CROTYLTRI-N-BUTYLSTANNANE ADDITIONS TO α-ALKOXY ALDEHYDES. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435110
KECK, G. E., ABBOTT, D. E., BODEN, E. P., ENHOLM, E. J. (1985) ChemInform Abstract: OBSERVATIONS ON THE CHOICE OF LEWIS ACID AND MODE OF ADDITION FOR THE LEWIS ACID-MEDIATED REACTION OF CROTYLTRI-N-BUTYLSTANNANE WITH ALDEHYDES: CONVENIENT AND HIGHLY SELECTIVE ACCESS TO BOTH ERYTHRO AND THREO PRODUCTS. Chemischer Informationsdienst, 16 (3) doi:10.1002/chin.198503162
KECK, G. E., YATES, J. B. (1983) ChemInform Abstract: HYDROGEN TRANSFER FROM CROTYLTRI-N-BUTYLSTANNANE TO CARBON RADICALS. Chemischer Informationsdienst, 14 (39) doi:10.1002/chin.198339147
KECK, G. E., BODEN, E. P. (1984) ChemInform Abstract: Stereocontrolled Additions of Allyltri-n-butylstannane to α-Hydroxyaldehyde Derivatives. A Useful Route to Monoprotected erythro or threo Diols. Chemischer Informationsdienst, 15 (20) doi:10.1002/chin.198420159
MAYR, H., KLEIN, H., KOLBERG, G. (1984) ChemInform Abstract: LEWIS ACID CATALYZED ADDITIONS OF 1,3-ALKYL SUBSTITUTED ALLYL CHLORIDES TO ALKENES. Chemischer Informationsdienst, 15 (46) doi:10.1002/chin.198446109
MUKAIYAMA, T., IWASAWA, N. (1983) ChemInform Abstract: STANNOUS TRIFLATE MEDIATED ALDOL REACTION OF 3-ACYLTHIAZOLIDINE-2-THIONE: A CONVENIENT METHOD FOR THE STEREOSELECTIVE SYNTHESES OF β-HYDROXY ALDEHYDE AND β-HYDROXY CARBOXYLIC ACID DERIVATIVES. Chemischer Informationsdienst, 14 (23) doi:10.1002/chin.198323234
KECK, G. E., ENHOLM, E. J., KACHENSKY, D. F. (1984) ChemInform Abstract: TWO NEW METHODS FOR THE SYNTHESIS OF C-GLYCOSIDES. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435329
KECK, G. E., KACHENSKY, D. F., ENHOLM, E. J. (1984) ChemInform Abstract: TOTAL SYNTHESIS OF PSEUDOMONIC ACID C. Chemischer Informationsdienst, 15 (39) doi:10.1002/chin.198439312
KECK, G. E., CASTELLINO, S. (1986) ChemInform Abstract: On the Origins of Stereoselectivity in "Chelation Controlled" Nucleophilic Additions to β-Alkoxy Aldehydes: Solution Structures of Lewis Acid Complexes via NMR Spectroscopy. Chemischer Informationsdienst, 17 (42) doi:10.1002/chin.198642064
FRATER, G., MUELLER, U., GUENTHER, W. (1984) ChemInform Abstract: THE STEREOSELECTIVE α-ALKYLATION OF CHIRAL β-HYDROXY ESTERS AND SOME APPLICATIONS THEREOF. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435099
HUYBRECHTS, L., BUFFEL, D., FREYNE, E., HOORNAERT, G. (1984) ChemInform Abstract: THE SYNTHESIS OF 5-CARBOXAMIDO-4-HYDROXY-3-(β-D-RIBOFURANOSYL)THIOPHENE DERIVATIVES, ANALOGS OF PYRAZOFURIN. Chemischer Informationsdienst, 15 (43) doi:10.1002/chin.198443341
 
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