Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method

Astellifadiene: Structure Determination by NMR Spectroscopy and Crystalline Sponge Method, and Elucidation of its Biosynthesis

(2016) Yudai Matsuda et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Determination of the Absolute Configuration of the Pseudo-Symmetric Natural Product Elatenyne by the Crystalline Sponge Method

(2016) Sylvia Urban et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Structure determination of microbial metabolites by the crystalline sponge method

(2016) Yasuhide Inokuma et al.   Chemical Science

The crystalline sponge method updated

(2016) Manabu Hoshino et al.   IUCrJ

Where is the Oxygen? Structural Analysis of α-Humulene Oxidation Products by the Crystalline Sponge Method

(2015) Nicolas Zigon et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method

(2015) Shota Yoshioka et al.   Chemical Science

Analysis of rapidly synthesized guest-filled porous complexes with synchrotron radiation: practical guidelines for the crystalline sponge method

(2015) Timothy R. Ramadhar et al.   Acta Crystallographica A-Foundation and Advances

Preparation and guest-uptake protocol for a porous complex useful for 'crystal-free' crystallography

(2014) Yasuhide Inokuma et al.   Nature Protocols

Palladium-Catalyzed Asymmetric Construction of Vicinal All-Carbon Quaternary Stereocenters and its Application to the Synthesis of Cyclotryptamine Alkaloids

(2013) Barry M. Trost et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles

(2013) Kohsuke Ohmatsu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Biomedical Importance of Indoles

(2013) Nagendra Kaushik et al.   MOLECULES

X-ray analysis on the nanogram to microgram scale using porous complexes

(2013) Yasuhide Inokuma et al.   NATURE

Organocatalyzed Formal [2 + 2] Cycloaddition of Ketimines with Allenoates: Facile Access to Azetidines with a Chiral Tetrasubstituted Carbon Stereogenic Center

(2013) Shinobu Takizawa et al.   ORGANIC LETTERS

Use of intensity quotients and differences in absolute structure refinement

(2013) Simon Parsons et al.   Acta Crystallographica Section B-Structural Science Crystal Engineering and Materials

Catalytic Asymmetric Total Synthesis of Chimonanthine, Folicanthine, and Calycanthine through Double Michael Reaction of Bisoxindole

(2012) Harunobu Mitsunuma et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Enantioselective Synthesis of α-Alkylidene-γ-Butyrolactones: Intramolecular Rauhut-Currier Reaction Promoted by Acid/Base Organocatalysts

(2012) Shinobu Takizawa et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Morita–Baylis–Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs

(2012) Claudio G. Lima–Junior et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems

(2011) Jaya Prakash Das et al.   CHEMICAL COMMUNICATIONS

Metal-catalyzed asymmetric conjugate addition reaction: formation of quaternary stereocenters

(2010) Christine Hawner et al.   CHEMICAL COMMUNICATIONS

Recent Contributions from the Baylis−Hillman Reaction to Organic Chemistry

(2010) Deevi Basavaiah et al.   CHEMICAL REVIEWS

What made sesquiterpene lactones reach cancer clinical trials?

(2010) Akram Ghantous et al.   DRUG DISCOVERY TODAY

Using thet-distribution to improve the absolute structure assignment with likelihood calculations

(2010) Rob W. W. Hooft et al.   JOURNAL OF APPLIED CRYSTALLOGRAPHY

aza-Baylis−Hillman Reaction

(2009) Valérie Declerck et al.   CHEMICAL REVIEWS

The determination of the absolute configurations of chiral molecules using vibrational circular dichroism (VCD) spectroscopy

(2007) Philip J. Stephens et al.   CHIRALITY