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ChemInform Abstract: Efficient Synthesis of 7-, 8-, and 9-Membered Cyclic Allyltitanium Compounds and Their Stereoselective Addition Reaction with Aldehydes and Imines.

โœ Scribed by S. HIKICHI; Y. GAO; F. SATO


Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
28
Category
Article
ISSN
0931-7597

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โœฆ Synopsis


Efficient Synthesis of 7-, 8-, and 9-Membered Cyclic Allyltitanium Compounds and Their Stereoselective Addition Reaction with Aldehydes and Imines.

-The reaction of the cyclic allylic compounds (I) with in situ generated (ฮท2-propene)Ti(O-iPr)2 gives allylic titanium compounds via an oxidative pathway. Quenching with aldehydes results in syn-selective formation of cycloalkenyl alcohols. Interestingly, quenching with the imine (V) gives a high anti-selectivity for the resulting amines. -(HIKICHI, S.; GAO,


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