New facile synthesis of furan-2(3H)-ones and 2,3,5-trisubstituted furans via intramolecular Wittig reaction of acid anhydride

Tetrahedron ◽  
2019 ◽  
Vol 75 (25) ◽  
pp. 3441-3447 ◽  
Author(s):  
Mei Sun ◽  
Qin Wan ◽  
Ming-Wu Ding
Keyword(s):  
Wittig Reaction ◽  
Acid Anhydride ◽  
Facile Synthesis ◽  
Intramolecular Wittig Reaction ◽  
Trisubstituted Furans

Strategic Exploitation of the Wittig Reaction: Facile Synthesis of Heteroaromatics and Multifunctional Olefins

Synlett ◽  
2018 ◽  
Vol 29 (20) ◽  
pp. 2608-2622 ◽  
Author(s):  
Wenwei Lin ◽  
Praneeth Karanam ◽  
Ganapuram Reddy
Keyword(s):  
Wittig Reaction ◽  
Coumarin Derivatives ◽  
Facile Synthesis ◽  
Diversity Oriented Synthesis ◽  
New Methods ◽  
Intramolecular Wittig Reaction ◽  
New Synthesis ◽  
Wide Range ◽  
Industrial Level ◽  
New Strategies

In this account, our group’s efforts towards exploring new substrates as precursors for the Wittig reaction have been discussed. Several new strategies developed by our group for the generation of requisite ylides for the Wittig reaction are highlighted. The idea behind the development of some chemoselective and diversity-oriented strategies are discussed in detail in a progressive manner. These strategies encompass a wide range of substrates that are employed for the synthesis of an array of heterocycles and multifunctional olefins and present a huge scope for their application on an industrial level.1 Introduction2 Development of New Methods to Effect Intramolecular Wittig Reaction3 Development of a Catalytic Wittig Reaction4 New Synthesis of Bis-Heteroarenes5 Direct β-Acylation of 2-Arylidene-1,3-indandiones6 Doubly Chemoselective Protocol for the Diversity-Oriented Synthesis of Coumarin Derivatives7 Conclusion

scholarly journals Stereoselective Synthesis of Tetraalkyl Cyclobutene-1,2,3,4-tetracarboxylates. Synthesis of Tetraalkyl (Z,Z)-Buta-1,3-diene-1,2,3,4-tetracarboxylates

1999 ◽  
Vol 23 (8) ◽  
pp. 512-513
Author(s):  
Issa Yavari ◽  
Farahnaz Nourmohammadian
Keyword(s):  
Ring Opening ◽  
Wittig Reaction ◽  
Stereoselective Synthesis ◽  
Intramolecular Wittig Reaction ◽  
Ring Opening Reactions ◽  
Boiling Toluene

Tetraalkyl cyclobutene-1,2,3,4-tetracarboxylates, prepared by intramolecular Wittig reaction between a vinylphosphonium salt and diethyl 2-oxobutanedioate, undergo electrocyclic ring-opening reactions, in boiling toluene, to produce highly electron-deficient 1,3-dienes.

ChemInform Abstract: SYNTHESIS OF HETEROCYCLES BY AN INTRAMOLECULAR WITTIG REACTION

1980 ◽  
Vol 11 (49) ◽  
Author(s):  
K. NICKISCH ◽  
W. KLOSE ◽  
E. NORDHOFF ◽  
F. BOHLMANN
Keyword(s):  
Wittig Reaction ◽  
Intramolecular Wittig Reaction
Sign in / Sign up

Export Citation Format

Share Document