One-Pot Preparation of Functionalized Azabicyclo[6.3.0]alkanone Amino Acids by Tandem Cross Enyne Metathesis/Ring-Closing Metathesis

2020 ◽  
Vol 2020 (24) ◽  
pp. 3568-3575
Author(s):  
Eric Bernardi ◽  
Lino Colombo ◽  
Ersilia De Lorenzi ◽  
Massimo Carraro ◽  
Massimo Serra
2020 ◽  
Vol 53 (11) ◽  
pp. 4330-4337
Author(s):  
Santhosh Kumar Podiyanachari ◽  
Salvador Moncho ◽  
Edward N. Brothers ◽  
Saeed Al-Meer ◽  
Mohammed Al-Hashimi ◽  
...  

2021 ◽  
Author(s):  
Lamiaa Reda Ahmed ◽  
Ahmed F. M. EL-Mahdy ◽  
Cheng-Tang Pan ◽  
Shiao-Wei Kuo

In this paper, we describe the construction of a new fluorescent hydroxyl- and hydrazone-based covalent organic framework (TFPB-DHTH COF) through the one-pot polycondensation of 1,3,5-tris(4-formylphenyl)benzene (TFPB) and 2,5-dihydroxyterephthalohydrazide (DHTH) under...


2016 ◽  
Vol 14 (2) ◽  
pp. 556-563 ◽  
Author(s):  
Veladi Panduranga ◽  
Girish Prabhu ◽  
Roopesh Kumar ◽  
Basavaprabhu Basavaprabhu ◽  
Vommina V. Sureshbabu

A simple and efficient method for the synthesis of N,N’-orthogonally protected imide tethered peptidomimetics is presented. The imide peptidomimetics were synthesized by coupling the in situ generated selenocarboxylate of Nα-protected amino acids with Nα-protected amino acid azides in good yields.


2016 ◽  
Vol 14 (44) ◽  
pp. 10473-10480 ◽  
Author(s):  
Sylvain Daunay ◽  
Remi Lebel ◽  
Laurence Farescour ◽  
Jean-Claude Yadan ◽  
Irene Erdelmeier

Natural and novel sulfur-containing amino acids are preparedviaa new regioselective one-pot two-step procedure.


2005 ◽  
Vol 11 (3) ◽  
pp. 849-862 ◽  
Author(s):  
Hiroshi Tanaka ◽  
Masaatsu Adachi ◽  
Takashi Takahashi

2004 ◽  
Vol 2004 (4) ◽  
pp. 800-806 ◽  
Author(s):  
Sofia S. Salim ◽  
Richard K. Bellingham ◽  
Richard C. D. Brown

Author(s):  
Satoru Arimitsu ◽  
Gerald B Hammond

gem-Difluoro-1,7-enyne amides are suitable building blocks for the synthesis of difluorodihydropyridinones via a ring-closing metathesis reaction, and of 4,4-difluoro-3-oxoisoquinolines through a ring-closing metathesis–enyne metathesis tandem reaction. These products, in turn, undergo a Diels–Alder reaction to yield heterotricyclic systems in moderate to good yields.


2005 ◽  
Vol 2005 (16) ◽  
pp. 3461-3468 ◽  
Author(s):  
Alicia Boto ◽  
Yolanda De León ◽  
Juan Antonio Gallardo ◽  
Rosendo Hernández
Keyword(s):  

ChemInform ◽  
2003 ◽  
Vol 34 (26) ◽  
Author(s):  
Arantxa Rodriguez ◽  
David D. Miller ◽  
Richard F. W. Jackson

Sign in / Sign up

Export Citation Format

Share Document