Recent developments in methods for the esterification and protection of the carboxyl group

E Haslam - Tetrahedron, 1980 - Elsevier
The chemistry of the carboxyl group is one of the cornerstones of organic chemistry. As a
consequence two very important facets of synthetic methodology are the activation of the …

[图书][B] Principles of peptide synthesis

M Bodanszky - 2012 - books.google.com
A look at the shelves of a major library awakens doubts in the author of this small volume
about the importance of writing a new introduction to peptide synthesis. This rather narrow …

Synthetic approaches to selenoesters

LL Baldassari, DS Lüdtke - Chemistry–A European Journal, 2021 - Wiley Online Library
Selenoesters are compounds of great synthetic relevance since they can be used in several
types of chemical transformations and mainly due to their great capacity in the formation of …

Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins

YF Zeng, DH Tan, Y Chen, WX Lv, XG Liu… - Organic Chemistry …, 2015 - pubs.rsc.org
A mild and convenient oxidative radical cyclization of aryl alkynoate esters for the synthesis
of 3-trifluoromethylthiolated and 3-thiocyanated coumarins has been developed using …

Umpolung Synthesis of Selenoesters and Telluroesters via the Photoinduced Coupling of Acylsilanes with Electrophilic Chalcogen Reagents

R Masuda, Y Anami, H Kusama - Organic Letters, 2024 - ACS Publications
A novel synthesis of selenoesters and telluroesters based on the reactions of nucleophilic
siloxycarbenes, which were generated by the visible-light-induced isomerization of the …

General, mild, and metal-free synthesis of phenyl selenoesters from anhydrides and their use in peptide synthesis

A Temperini, F Piazzolla, L Minuti… - The Journal of …, 2017 - ACS Publications
A mild, practical, and simple procedure for phenyl selenoesters synthesis from several
anhydrides and diphenyl diselenide was developed. This transition-metal-free method …

Selective electrochemical para-thiocyanation of aromatic amines under metal-, oxidant-and exogenous-electrolyte-free conditions

Y Zhang, H Gao, J Guo, H Zhang, X Yao - Chemical Communications, 2021 - pubs.rsc.org
An electrochemical oxidative para-C–H-thiocyanation of aromatic amines has been
developed to construct thiocyanato aromatic compounds under metal-, oxidant-, and …

N-phenylselenophthalimide (NPSP): a valuable selenenylating agent

KC Nicolaou, NA Petasis, DA Claremon - Tetrahedron, 1985 - Elsevier
The phenylseleno group (PhSe) has evolved in recent years as a very useful and versatile
functionality. Its facile introduction into organic molecules and its subsequent oxidative or …

Novel selenoesters fluorescent liquid crystalline exhibiting a rich phase polymorphism

DS Rampon, FS Rodembusch… - Journal of Materials …, 2010 - pubs.rsc.org
A simple and efficient procedure for the synthesis of a new class of selenoesters 4a and 4b
was developed. Polarized-light optical microscopy (POM), differential scanning calorimetry …

Access to saturated thiocyano-containing azaheterocycles via selenide-catalyzed regio-and stereoselective thiocyanoaminocyclization of alkenes

W Wei, L Liao, T Qin, X Zhao - Organic letters, 2019 - ACS Publications
An efficient route for the synthesis of saturated thiocyano-containing azaheterocycles by
selenide-catalyzed regio-and stereoselective thiocyanoaminocyclization of alkenes is …