Highly Efficient Ring Closure of Aromatic Dialdehydes to Macrocyclic Allenes

1997 ◽  
Vol 119 (15) ◽  
pp. 3429-3433 ◽  
Author(s):  
Marcus S. Brody ◽  
Robin M. Williams ◽  
M. G. Finn
Keyword(s):  
Ring Closure ◽  
Highly Efficient

A Highly Efficient Synthesis of Lamellarins K and L by the Michael Addition/Ring-Closure Reaction of Benzyldihydroisoquinoline Derivatives with Ethoxycarbonyl-β-nitrostyrenes

2004 ◽  
Vol 116 (7) ◽  
pp. 884-886 ◽  
Author(s):  
Poonsakdi Ploypradith ◽  
Chulabhorn Mahidol ◽  
Poolsak Sahakitpichan ◽  
Siriporn Wongbundit ◽  
Somsak Ruchirawat
Keyword(s):  
Michael Addition ◽  
Ring Closure ◽  
Efficient Synthesis ◽  
Highly Efficient ◽  
The Michael Addition

Ruthenium catalysts bearing a benzimidazolylidene ligand for the metathetical ring-closure of tetrasubstituted cycloolefins

2015 ◽  
Vol 44 (21) ◽  
pp. 9744-9755 ◽  
Author(s):  
Yannick Borguet ◽  
Guillermo Zaragoza ◽  
Albert Demonceau ◽  
Lionel Delaude
Keyword(s):  
Second Generation ◽  
Ruthenium Catalysts ◽  
Ring Closure ◽  
Ring Closing Metathesis ◽  
Highly Efficient ◽  
Alkylidene Complexes

Second-generation ruthenium–alkylidene complexes featuring the 1,3-di(2-tolyl)benzimidazol-2-ylidene ligand (BTol) are highly efficient catalysts for the synthesis of tetrasubstituted cycloolefins via ring-closing metathesis (RCM).

ChemInform Abstract: Highly Efficient Ring Closure of Aromatic Dialdehydes to Macrocyclic Allenes.

ChemInform ◽  
2010 ◽  
Vol 28 (32) ◽  
pp. no-no
Author(s):  
M. S. BRODY ◽  
R. M. WILLIAMS ◽  
M. G. FINN
Keyword(s):  
Ring Closure ◽  
Highly Efficient

A Highly Efficient Synthesis of Lamellarins K and L by the Michael Addition/Ring-Closure Reaction of Benzyldihydroisoquinoline Derivatives with Ethoxycarbonyl-β-nitrostyrenes

2004 ◽  
Vol 43 (7) ◽  
pp. 866-868 ◽  
Author(s):  
Poonsakdi Ploypradith ◽  
Chulabhorn Mahidol ◽  
Poolsak Sahakitpichan ◽  
Siriporn Wongbundit ◽  
Somsak Ruchirawat
Keyword(s):  
Michael Addition ◽  
Ring Closure ◽  
Efficient Synthesis ◽  
Highly Efficient ◽  
The Michael Addition

A Highly Efficient Synthesis of Lamellarins K (Ia) and L (Ib) by the Michael Addition/Ring-Closure Reaction of Benzyldihydroisoquinoline Derivatives with Ethoxycarbonyl-β-nitrostyrenes.

ChemInform ◽  
2004 ◽  
Vol 35 (24) ◽  
Author(s):  
Poonsakdi Ploypradith ◽  
Chulabhorn Mahidol ◽  
Poolsak Sahakitpichan ◽  
Siriporn Wongbundit ◽  
Somsak Ruchirawat
Keyword(s):  
Michael Addition ◽  
Ring Closure ◽  
Efficient Synthesis ◽  
Highly Efficient ◽  
The Michael Addition

Highly efficient and selective photocatalytic CO2 to CO conversion in aqueous solution

2020 ◽  
Vol 56 (27) ◽  
pp. 3851-3854 ◽  
Author(s):  
Xiaomin Chai ◽  
Hai-Hua Huang ◽  
Huiping Liu ◽  
Zhuofeng Ke ◽  
Wen-Wen Yong ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Performance ◽  
Aqueous Media ◽  
Highly Efficient ◽  
Co Conversion

A Co-based complex displayed the highest photocatalytic performance for CO2 to CO conversion in aqueous media.

Tuning the pore structures and photocatalytic properties of a 2D covalent organic framework with multi-branched photoactive moieties

Nanoscale ◽  
2020 ◽  
Vol 12 (30) ◽  
pp. 16136-16142
Author(s):  
Xuan Wang ◽  
Ming-Jie Dong ◽  
Chuan-De Wu
Keyword(s):  
Photocatalytic Properties ◽  
Effective Strategy ◽  
Covalent Organic Framework ◽  
Highly Efficient ◽  
Pore Structures ◽  
Local Connection ◽  
Organic Framework

An effective strategy to incorporate accessible metalloporphyrin photoactive sites into 2D COFs by establishing a 3D local connection for highly efficient photocatalysis was developed.

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