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N-(Boc)-6-fluoroindole-2-boronic acid

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For Research Use Only | Not For Clinical Use
CATLS7931247
MDL NumberMFCD09953519
Molecular Weight279.07
InChI KeyGARRUKBUEWVRCV-UHFFFAOYSA-N
DescriptionAldrichCPR
Size100MG
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Crystal structure of N-{ N-[ N-( tert-but-oxy-carbon-yl)-l-α-aspart-yl]-l-α-aspart-yl}-l-α-aspartic acid 1 4,2 4,3 4-trimethyl ester 3 1-2-oxo-2-phenyl-ethyl ester {Boc-[Asp(OMe)] 3-OPac}

Takuma Kato, Saki Kishimoto, Akiko Asano, Mitsunobu Doi

Acta Crystallogr E Crystallogr Commun. 2019 Apr 9;75(Pt 5):585-588.

PMID: 31110791

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Diastereo- And Enantioseparation of a N(α)-Boc Amino Acid With a Zwitterionic Quinine-Based Stationary Phase: Focus on the Stereorecognition Mechanism

Federica Ianni, Andrea Carotti, Maura Marinozzi, Gloria Marcelli, Alessandro Di Michele, Roccaldo Sardella, Wolfgang Lindner, Benedetto Natalini

Anal Chim Acta. 2015 Jul 23;885:174-82.

PMID: 26231903

1

Kinetics and Mechanism of N-Boc Cleavage: Evidence of a Second-Order Dependence Upon Acid Concentration

Ian W Ashworth, Brian G Cox, Brian Meyrick

J Org Chem. 2010 Dec 3;75(23):8117-25.

PMID: 21067172

1

Preparation and Intramolecular [2+2]-photocycloaddition of 1,5-dihydropyrrol-2-ones and 5,6-dihydro-1H-pyridin-2-ones With C-, N-, and O-linked Alkenyl Side Chains at the 4-position

Dominik Albrecht, Birte Basler, Thorsten Bach

J Org Chem. 2008 Mar 21;73(6):2345-56.

PMID: 18302416

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Synthesis of Enantiomerically Pure N-Boc-Protected 1,2,3-Triaminopropylphosphonates and 1,2-Diamino-3-Hydroxypropylphosphonates

Aleksandra Trocha, Dorota G Piotrowska, Iwona E Głowacka

Molecules. 2019 Oct 25;24(21):3857.

PMID: 31731561

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