Absolute configuration of an axially chiral sulfonate determined from its optical rotatory dispersion, electronic circular dichroism, and vibrational circular dichroism spectra.

about

Absolute configuration of an axially chiral sulfonate determined from its optical rotatory dispersion, electronic circular dichroism, and vibrational circular dichroism spectra.

Item

http://www.wikidata.org/entity/Q48192403

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Absolute configuration of an a ...... al circular dichroism spectra.

@en

Absolute configuration of an a ...... al circular dichroism spectra.

@nl

type

Item

label

Absolute configuration of an a ...... al circular dichroism spectra.

@en

Absolute configuration of an a ...... al circular dichroism spectra.

@nl

prefLabel

Absolute configuration of an a ...... al circular dichroism spectra.

@en

Absolute configuration of an a ...... al circular dichroism spectra.

@nl

P1476

Absolute configuration of an a ...... nal circular dichroism spectra

@en

P2093

Cody L Covington

http://www.w3.org/2001/XMLSchema#string

Daniel W Armstrong

http://www.w3.org/2001/XMLSchema#string

Jonathan P Smuts

http://www.w3.org/2001/XMLSchema#string

Vijay Raghavan

http://www.w3.org/2001/XMLSchema#string

P2860

Structure and Stereochemical Determination of Hypogeamicins from a Cave-Derived Actinomycete.

Enantioselective C-H crotylation of primary alcohols via hydrohydroxyalkylation of butadiene

The calculations of excited-state properties with Time-Dependent Density Functional Theory.

Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra.

Absolute configurations of phytotoxic inuloxins B and C based on experimental and computational analysis of chiroptical properties.

A single chiroptical spectroscopic method may not be able to establish the absolute configurations of diastereomers: dimethylesters of hibiscus and garcinia acids.

Chiral-anion-dependent inversion of diastereo- and enantioselectivity in carbonyl crotylation via ruthenium-catalyzed butadiene hydrohydroxyalkylation.

A novel computational method for comparing vibrational circular dichroism spectra.

Enantiomeric separations of chiral sulfonic and phosphoric acids with barium-doped cyclofructan selectors via an ion interaction mechanism.

Configurationally Stable Chiral Dithia-Bridged Hetero[4]helicene Radical Cation: Electronic Structure and Absolute Configuration.

P304

670-676

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/CHIR.22739

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Prasad L. Polavarapu

P577

2017-08-18T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28833487

http://www.w3.org/2001/XMLSchema#string