scholarly journals Direct Synthesis Sulfonamides from Nitroarenes and Sulfonyl Chlorides in Water

2019 ◽  
Vol 39 (2) ◽  
pp. 463 ◽  
Author(s):  
Huilan Yue ◽  
Pengli Bao ◽  
Leilei Wang ◽  
Xiaoxia Lü ◽  
Daoshan Yang ◽  
...  
Keyword(s):  
Direct Synthesis ◽  
Sulfonyl Chlorides

Tertiary amine-catalyzed and direct synthesis of α-chloroalkanesulfonylhydrazines from azodicarboxylates and sulfonyl chlorides

2016 ◽  
Vol 14 (21) ◽  
pp. 4918-4926 ◽  
Author(s):  
Bingnan Zhou ◽  
Jiaxi Xu
Keyword(s):  
Tertiary Amine ◽  
Direct Synthesis ◽  
Tertiary Amines ◽  
Sulfonyl Chlorides

α-Chloroalkanesulfonylhydrazines were synthesized directly and efficiently from alkanesulfonyl chlorides and dialkyl azodicarboxylates under the catalysis of tertiary amines.

Direct synthesis of thioethers from sulfonyl chlorides and activated alcohols

2002 ◽  
Vol 43 (12) ◽  
pp. 2145-2147 ◽  
Author(s):  
Michael T Martin ◽  
Alford M Thomas ◽  
Douglas G York
Keyword(s):  
Direct Synthesis ◽  
Sulfonyl Chlorides

ChemInform Abstract: Direct Synthesis of Thioethers from Sulfonyl Chlorides and Activated Alcohols.

ChemInform ◽  
2010 ◽  
Vol 33 (27) ◽  
pp. no-no
Author(s):  
Michael T. Martin ◽  
Alford M. Thomas ◽  
Douglas G. York
Keyword(s):  
Direct Synthesis ◽  
Sulfonyl Chlorides

Direct synthesis of thiophosphates by reaction of diphenylphosphine oxide with sulfonyl chlorides

Tetrahedron ◽  
2016 ◽  
Vol 72 (47) ◽  
pp. 7594-7598 ◽  
Author(s):  
Wei He ◽  
Zhiming Wang ◽  
Xinjin Li ◽  
Qing Yu ◽  
Zhongwei Wang
Keyword(s):  
Direct Synthesis ◽  
Diphenylphosphine Oxide ◽  
Sulfonyl Chlorides

Palladium-catalyzed carbonylative transformation of aryl iodides and sulfonyl chlorides: convenient access to thioesters

2020 ◽  
Vol 7 (6) ◽  
pp. 885-889 ◽  
Author(s):  
Xinxin Qi ◽  
Zhi-Peng Bao ◽  
Xiao-Feng Wu
Keyword(s):  
Sulfonyl Chlorides ◽  
Aryl Iodides ◽  
Palladium Catalyzed ◽  
Convenient Access

A palladium-catalyzed carbonylative transformation of aryl iodides and sulfonyl chlorides to thioesters has been studied.

Structure Guided Molecular Docking Assisted Alignment Dependent 3DQSAR Study on Steroidal Aromatase Inhibitors (SAIs) as Anti-breast Cancer Agents

2019 ◽  
Vol 16 (7) ◽  
pp. 808-817 ◽  
Author(s):  
Laxmi Banjare ◽  
Sant Kumar Verma ◽  
Akhlesh Kumar Jain ◽  
Suresh Thareja
Keyword(s):  
Breast Cancer ◽  
Molecular Docking ◽  
Aromatase Inhibitors ◽  
Direct Synthesis ◽  
3D Qsar ◽  
Chemotherapeutic Agents ◽  
Modeling Tools ◽  
Data Set ◽  
Wide Range ◽  
Steroidal Aromatase Inhibitors

Background: In spite of the availability of various treatment approaches including surgery, radiotherapy, and hormonal therapy, the steroidal aromatase inhibitors (SAIs) play a significant role as chemotherapeutic agents for the treatment of estrogen-dependent breast cancer with the benefit of reduced risk of recurrence. However, due to greater toxicity and side effects associated with currently available anti-breast cancer agents, there is emergent requirement to develop target-specific AIs with safer anti-breast cancer profile. Methods: It is challenging task to design target-specific and less toxic SAIs, though the molecular modeling tools viz. molecular docking simulations and QSAR have been continuing for more than two decades for the fast and efficient designing of novel, selective, potent and safe molecules against various biological targets to fight the number of dreaded diseases/disorders. In order to design novel and selective SAIs, structure guided molecular docking assisted alignment dependent 3D-QSAR studies was performed on a data set comprises of 22 molecules bearing steroidal scaffold with wide range of aromatase inhibitory activity. Results: 3D-QSAR model developed using molecular weighted (MW) extent alignment approach showed good statistical quality and predictive ability when compared to model developed using moments of inertia (MI) alignment approach. Conclusion: The explored binding interactions and generated pharmacophoric features (steric and electrostatic) of steroidal molecules could be exploited for further design, direct synthesis and development of new potential safer SAIs, that can be effective to reduce the mortality and morbidity associated with breast cancer.

α-Ketophosphonates in the Synthesis of α-iminophosphonates

2020 ◽  
Vol 7 (2) ◽  
pp. 226-238
Author(s):  
Petro P. Ony`sko ◽  
Tetyana I. Chudakova ◽  
Vladimir V. Pirozhenko ◽  
Alexandr B. Rozhenko
Keyword(s):  
Bond Cleavage ◽  
Direct Synthesis ◽  
Equilibrium Mixture ◽  
Primary Amines ◽  
Alkyl Amines ◽  
Protic Solvents ◽  
Metallic Salts ◽  
Direct Preparation ◽  
Stage Synthesis ◽  
Aprotic Dipolar Solvent

The potentialities of condensation of α-ketophosphonates with primary amines for direct synthesis of α-iminophosphonates have been revealed. Diesters of α-ketophosphonic acids react with the primary amines by two competitive pathways: with a formation of α-iminophosphonates or a C-P bond cleavage resulting in a hydrogen phosphonate and an acylated amine. In many cases, the latter undesirable pathway is dominant, especially for more nucleophilic alkyl amines. Using metallic salts of α-ketophosphonates avoids the C-P bond cleavage, allowing direct preparation of α-phosphorylated imines by the reaction with primary amines. This strategy provides an atom economy single-stage synthesis of iminophosphonates – precursors of bio relevant phosphorus analogs of α-amino acids. Methyl sodium iminophosphonates, bearing aryl or heteryl substituents at the imino carbon atom exist in solutions at room temperature as an equilibrium mixture of Z- and E-isomers. A configuration of the C=N bond can be controlled by the solvent: changing the aprotic dipolar solvent DMSO-d6 by water or alcohols leads to the change from a predominant Z-isomer to almost an exclusive E-form. In contrast, diesters of the respective iminophosphonates exist in non-protic solvents predominantly in Econfiguration. The solvent effect on E-Z stereochemistry is demonstrated by DFT calculations.

Sign in / Sign up

Export Citation Format

Share Document