|Title:||N-Heterocyclic Carbene-Catalyzed Benzoin Strategy for Divergent Synthesis of Cyclitol Derivatives from Alditols|
Takasu, Kiyosei https://orcid.org/0000-0002-1798-7919 (unconfirmed)
|Author's alias:||高須, 清誠|
|Journal title:||Advanced Synthesis & Catalysis|
|Abstract:||A divergent synthesis of cyclitol derivatives has been developed utilizing an N-heterocyclic carbene-catalyzed benzoin-type cyclization of C2-symmetrical dialdoses. The resulting inososes are versatile intermediates, which are readily converted into not only inositols but also amino-, deoxy-, O-methyl- and C-methyl-inositols.|
|Rights:||This is the peer reviewed version of the following article: Kang, B., Sutou, T., Wang, Y., Kuwano, S., Yamaoka, Y., Takasu, K. and Yamada, K.-i. (2015), N-Heterocyclic Carbene-Catalyzed Benzoin Strategy for Divergent Synthesis of Cyclitol Derivatives from Alditols. Adv. Synth. Catal., 357: 131–147, which has been published in final form at http://dx.doi.org/10.1002/adsc.201400712. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.|
The full-text file will be made open to the public on 8 DEC 2015 in accordance with publisher's 'Terms and Conditions for Self-Archiving'
This is not the published version. Please cite only the published version.
|Appears in Collections:||Journal Articles|
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