Synthesis of the Sulfonate Analogue of Seminolipid via Horner−Wadsworth−Emmons Olefination-Reference-Cited by-同舟云学术

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Synthesis of the Sulfonate Analogue of Seminolipid via Horner−Wadsworth−Emmons Olefination

Published:2010-07-14 Issue:15 Volume:75 Page:5363-5366
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Franchini Laura¹,Compostella Federica¹,Colombo Diego¹,Panza Luigi²,Ronchetti Fiamma¹

Affiliation:

1. Dipartimento di Chimica, Biochimica e Biotecnologie per la Medicina, Università di Milano, Via Saldini 50, 20133-Milano, Italy

2. Dipartimento di Scienze Chimiche, Alimentari, Farmaceutiche e Farmacologiche, Università del Piemonte Orientale, Via Bovio 6, 28100-Novara, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo1008788

Reference32 articles.

1. The specific localization of seminolipid molecular species on mouse testis during testicular maturation revealed by imaging mass spectrometry

2. An efficient and convenient synthesis of deuterium-labelled seminolipid isotopomers and their ESI-MS characterization

3. Sperm capacitation induces an increase in lipid rafts having zona pellucida binding ability and containing sulfogalactosylglycerolipid

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1. Synthesis and Conformational Analyses of Cyclonucleoside Having 13-Membered Ring Bridging Nucleobase and 5′-Position via a Linker Containing Sulfonamide;Organic Letters;2023-10-19

2. Synthesis of 2′-O-[3-(N-methylsulfamoyl)propan-1-yl]ribothymidine as a potentially applicable 2′-modified nucleoside for antisense oligonucleotides;Bioorganic & Medicinal Chemistry;2022-11

3. Unusual promoters and leaving groups in glycosylation reactions: The evolution of carbohydrate synthesis;Carbohydrate Research;2022-09

4. Molecular Construction of Sulfonamide Antisense Oligonucleotides;The Journal of Organic Chemistry;2019-08-05

5. Total syntheses of seminolipid and its analogues by using 2,6-bis(trifluoromethyl)phenylboronic acid as protective reagent;Organic & Biomolecular Chemistry;2019

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