scholarly journals Straightforward N-alkylation of diketopyrrolopyrroles through Mitsunobu reaction with benzyl, α-branched, and chiral alcohols

2021 ◽  
Author(s):  
Maurizio Mastropasqua Talamo ◽  
FLAVIA POP ◽  
Narcis Avarvari
Keyword(s):  
Mitsunobu Reaction ◽  
Chiral Alcohols ◽  
Fundamental Step

The N-alkylation of diketopyrrolopyrroles (DPPs) represents a fundamental step to ensure solubility and further processability. Commonly used nucleophilic subtitution on halogenated derivatives is replaced in this work by Mitsunobu reaction...

An Organocatalytic Mitsunobu Reaction

2020 ◽  
Vol 2 (2) ◽  
pp. 174-175
Author(s):  
Benjamin T. Boyle ◽  
Kyle G. Nottingham ◽  
Andrew McNally
Keyword(s):  
Mitsunobu Reaction

Synthesis and characterization of novel chiral derivatizing agents containing β-keto-anthracene adducts (KAAs) by 1H-NMR: aromatic influence and chiral alcohol absolute configuration determination

2019 ◽  
Vol 17 (3) ◽  
pp. 541-554
Author(s):  
Neeranuth Intakaew ◽  
Puracheth Rithchumpon ◽  
Chanatkran Prommin ◽  
Saranphong Yimklan ◽  
Nawee Kungwan ◽  
...  
Keyword(s):  
1H Nmr ◽  
Absolute Configuration ◽  
Synthesis And Characterization ◽  
Chiral Alcohols ◽  
Chiral Alcohol ◽  
Aromatic Rings ◽  
H Nmr ◽  
Chiral Derivatizing Agents

New chiral derivatizing agents and the effect of aromatic rings were investigated for absolute configuration of chiral alcohols via1H-NMR.

Quantitative Coding of Negotiation Behavior

2004 ◽  
Vol 9 (3) ◽  
pp. 441-456 ◽  
Author(s):  
Laurie Weingart ◽  
Philip Smith ◽  
Mara Olekalns
Keyword(s):  
Data Analysis ◽  
Quantitative Data ◽  
Primary Source ◽  
Research Process ◽  
Fundamental Step ◽  
Coding Scheme ◽  
Negotiation Behavior ◽  
Negotiation Processes ◽  
Shed Light

AbstractThe examination of negotiation processes is seen by many researchers as an insurmountable task largely because the required methods are unfamiliar and labor-intensive. In this article, we shed light on a fundamental step in studying negotiation processes, the quantitative coding of data. Relying on videotapes as the primary source of data, we review the steps required to extract usable quantitative data and the lessons we've learned in doing so in our own research. We review our experience working with one large negotiation dataset, Towers Market II, to illustrate two steps within the larger research process: developing a coding scheme and coding the data. We then go on to discuss some of the issues that need to be resolved before data analysis begins.

The Mitsunobu Reaction of Tetrachlorophthalimide

Synlett ◽  
1999 ◽  
Vol 1999 (5) ◽  
pp. 565-566 ◽  
Author(s):  
Zhaozhong J. Jia ◽  
Sandra Kelberlau ◽  
Lars Olsson ◽  
G. Anilkumar ◽  
Bert Fraser-Reid
Keyword(s):  
Mitsunobu Reaction

Asymmetric Synthesis of Organophosphorus Compounds using H-P reagents derived from Chiral Alcohols

2021 ◽  
Author(s):  
Tomasz K. Olszewski ◽  
Joseph Gbubele
Keyword(s):  
Asymmetric Synthesis ◽  
Phosphorus Atom ◽  
Organophosphorus Compounds ◽  
Chiral Alcohols

Chiral organophosphorus compounds, especially those containing C-stereogenic carbons in the proximity of the phosphorus atom, are known for their unique properties and have found wide applications that span from medicinal...

Preparation of Structurally Diverse Chiral Alcohols by Engineering Ketoreductase CgKR1

ACS Catalysis ◽  
2017 ◽  
Vol 7 (10) ◽  
pp. 7174-7181 ◽  
Author(s):  
Gao-Wei Zheng ◽  
Yuan-Yang Liu ◽  
Qi Chen ◽  
Lei Huang ◽  
Hui-Lei Yu ◽  
...  
Keyword(s):  
Chiral Alcohols

CHIRAL ALCOHOLS

2008 ◽  
Vol 86 (50) ◽  
pp. 8
Author(s):  
SARAH EVERTS
Keyword(s):  
Chiral Alcohols

Preparation of 2,3-Dideoxy-2,3-epimino and 3,4-Dideoxy-3,4-epimino Derivatives of 1,6-Anhydro-β-D-hexopyranoses by Mitsunobu Reaction

1998 ◽  
Vol 63 (6) ◽  
pp. 813-825 ◽  
Author(s):  
Jiří Kroutil ◽  
Tomáš Trnka ◽  
Miloš Buděšínský ◽  
Miloslav Černý
Keyword(s):  
Nmr Spectra ◽  
Mitsunobu Reaction ◽  
Derivatives Of ◽  
C Nmr

A series of new 2-, 3- and 4-benzylamino-2-, 3- and 4-deoxy derivatives of 1,6-anhydro-β-D-hexopyranoses were prepared from 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses by treatment with benzylamine and converted into 2,3-(N-benzylepimino)-2,3-dideoxy- and 3,4-(N-benzylepimino)-3,4-dideoxy-β-D-hexopyranoses of the D-allo, D-galacto and D-talo configuration by Mitsunobu reaction. The structures of benzylamino and benzylimino derivatives were confirmed by 1H and 13C NMR spectra.

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