ChemInform Abstract: Copper(II) Acetate Catalyzed Ring-Opening Cross-Coupling of Cyclopropanols with Sulfonyl Azides.

ChemInform ◽  
2016 ◽  
Vol 47 (14) ◽  
Author(s):  
Mei-Hua Shen ◽  
Xiao-Long Lu ◽  
Hua-Dong Xu
Keyword(s):  
Ring Opening ◽  
Cross Coupling ◽  
Sulfonyl Azides

Copper(ii) acetate catalysed ring-opening cross-coupling of cyclopropanols with sulfonyl azides

RSC Advances ◽  
2015 ◽  
Vol 5 (120) ◽  
pp. 98757-98761 ◽  
Author(s):  
Mei-Hua Shen ◽  
Xiao-Long Lu ◽  
Hua-Dong Xu
Keyword(s):  
Ring Opening ◽  
Cross Coupling ◽  
Sulfonyl Azides ◽  
Sulfonyl Azide

A copper(ii) acetate catalyzed ring-opening cross-coupling of cyclopropanol with sulfonyl azide has been developed.

Design and synthesis of 1,8-Naphthalimide Functionalized Benzothiadiazoles

2021 ◽  
Author(s):  
Rajneesh Misra ◽  
Yogjivan Rout
Keyword(s):  
Ring Opening ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Design And Synthesis ◽  
Cross Coupling Reaction ◽  
Ring Opening Reaction

A series of multi acceptor based push-pull derivatives BTD2–BTD5 were designed and synthesized via Pd-catalyzed Sonogashira cross-coupling reaction followed by [2+2] cycloaddition–electrocyclic ring-opening reaction in which benzothiadiazole (BTD, A1), naphthalimide...

Pd‐Catalyzed Enantioselective Ring Opening/Cross‐Coupling and Cyclopropanation of Cyclobutanones

2018 ◽  
Author(s):  
Jian Cao ◽  
Ling Chen ◽  
Feng‐Na Sun ◽  
Yu‐Li Sun ◽  
Ke‐Zhi Jiang ◽  
...  
Keyword(s):  
Ring Opening ◽  
Cross Coupling

ChemInform Abstract: Efficient Synthesis of β-CF3/SCF3-Substituted Carbonyls via Copper-Catalyzed Electrophilic Ring-Opening Cross-Coupling of Cyclopropanols.

ChemInform ◽  
2015 ◽  
Vol 46 (36) ◽  
pp. no-no
Author(s):  
Yong Li ◽  
Zhishi Ye ◽  
Tabitha M. Bellman ◽  
Teng Chi ◽  
Mingji Dai
Keyword(s):  
Ring Opening ◽  
Cross Coupling ◽  
Efficient Synthesis

Ligand-Free Nickel-Catalyzed Reductive Allylic Defluorinative Cross-Coupling of α-Trifluoromethyl Alkenes with Epoxides

Synlett ◽  
2020 ◽  
Author(s):  
Chuan Wang ◽  
Zhiyang Lin ◽  
Yun Lan
Keyword(s):  
Ring Opening ◽  
Cross Coupling ◽  
Proton Donor ◽  
Mild Conditions ◽  
Ligand Free ◽  
High Yields ◽  
Radical Type

We report a reductive allylic defluorinative reaction of α-trifluoromethyl alkenes with terminal epoxides, which consists of an iodide-mediated regioselective ring opening and a nickel-catalyzed radical-type cross-coupling, providing diverse tertiary gem-difluorobishomoallylic alcohols in moderate to high yields. Notably, this reaction is conducted under mild conditions and requires no external ligand or proton donor.

Cu-Catalyzed hydrophosphorylative ring opening of propargyl epoxides: highly selective access to 4-phosphoryl 2,3-allenols

2016 ◽  
Vol 52 (80) ◽  
pp. 11959-11962 ◽  
Author(s):  
Ruwei Shen ◽  
Jianlin Yang ◽  
Haipeng Zhao ◽  
Yu Feng ◽  
Lixiong Zhang ◽  
...  
Keyword(s):  
Ring Opening ◽  
Cross Coupling ◽  
Mild Conditions ◽  
Selective Access ◽  
Excellent Selectivity

A CuI-catalyzed cross-coupling of propargyl epoxides with P(O)H compounds to produce 4-phosphoryl 2,3-allenols with excellent selectivity under mild conditions is disclosed.

Regio- and stereoselective ring-opening dimerization–cross-coupling metathesis of 7-oxanorbornene derivatives

2001 ◽  
Vol 627 (1) ◽  
pp. 105-108 ◽  
Author(s):  
Odón Arjona* ◽  
Aurelio G Csákÿ ◽  
M.Carmen Murcia ◽  
Joaquı́n Plumet* ◽  
M.Belén Mula
Keyword(s):  
Ring Opening ◽  
Cross Coupling
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