ChemInform Abstract: Chiral Silicon Lewis Acids Having a Pentacoordinate Stereogenic Silicon Center: <sup>29</sup>Si NMR Studies and Application to Asymmetric Diels—Alder Reactions.

Sakaguchi, Yuhsuke; Iwade, Yuhki; Sekikawa, Tohru; Minami, Tatsuya; Hatanaka, Yasuo

doi:10.1002/chin.201416034

ChemInform

2014

DOI: 10.1002/chin.201416034

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ChemInform Abstract: Chiral Silicon Lewis Acids Having a Pentacoordinate Stereogenic Silicon Center: ²⁹Si NMR Studies and Application to Asymmetric Diels—Alder Reactions.

Yuhsuke Sakaguchi

Yuhki Iwade

Tohru Sekikawa

et al.

Abstract: NMR Studies reveal that chiral pentacoordinate silyl triflimides derived from BINOL derivatives (I) with a silicon stereogenic center are highly configurationally unstable.

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ChemInform Abstract: Chiral Silicon Lewis Acids Having a Pentacoordinate Stereogenic Silicon Center: ²⁹Si NMR Studies and Application to Asymmetric Diels—Alder Reactions.

Abstract: NMR Studies reveal that chiral pentacoordinate silyl triflimides derived from BINOL derivatives (I) with a silicon stereogenic center are highly configurationally unstable.

Cited by 0 publications

References 1 publication

No citations

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ChemInform Abstract: Chiral Silicon Lewis Acids Having a Pentacoordinate Stereogenic Silicon Center: 29Si NMR Studies and Application to Asymmetric Diels—Alder Reactions.

Abstract: NMR Studies reveal that chiral pentacoordinate silyl triflimides derived from BINOL derivatives (I) with a silicon stereogenic center are highly configurationally unstable.

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: Chiral Silicon Lewis Acids Having a Pentacoordinate Stereogenic Silicon Center: ²⁹Si NMR Studies and Application to Asymmetric Diels—Alder Reactions.