ChemInform Abstract: Enantioselective Synthesis of 2-Methyl-1,2-syn- and...

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ChemInform 2010, 41, issue 08 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Alcohols P 0110 DOI: 10.1002/chin.201008052 Enantioselective Synthesis of 2-Methyl-1,2-syn- and 2-Methyl-1,2-anti-3-butene- diols via Allene Hydroboration—Aldehyde Allylboration Reaction Sequences. Variation of the temperature in the hydroboration step allows selective formation of 1,2-syn- or 1,2-anti-3-butenediols. — (CHEN, M.; HANDA, M.; ROUSH*, W. R.; J. Am. Chem. Soc. 131 (2009) 41, 14602-14603; Dep. Chem., Scripps Florida, Jupiter, FL 33458, USA; Eng.) — Jannicke 08- 052

Transcript of ChemInform Abstract: Enantioselective Synthesis of 2-Methyl-1,2-syn- and...

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AlcoholsP 0110 DOI: 10.1002/chin.201008052

Enantioselective Synthesis of 2-Methyl-1,2-syn- and 2-Methyl-1,2-anti-3-butene-diols via Allene Hydroboration—Aldehyde Allylboration Reaction Sequences. — Variation of the temperature in the hydroboration step allows selective formation of 1,2-syn- or 1,2-anti-3-butenediols. — (CHEN, M.; HANDA, M.; ROUSH*, W. R.; J. Am. Chem. Soc. 131 (2009) 41, 14602-14603; Dep. Chem., Scripps Florida, Jupiter, FL 33458, USA; Eng.) — Jannicke

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ChemInform 2010, 41, issue 08 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim