ChemInform Abstract: Functionalization of an sp3C-H Bond via a Redox-Neutral Domino Reaction: Diastereoselective Synthesis of Hexahydropyrrolo[2,1-b]oxazoles.

ChemInform ◽  
2014 ◽  
Vol 45 (28) ◽  
pp. no-no
Author(s):  
Matiur Rahman ◽  
Avik Kumar Bagdi ◽  
Subhajit Mishra ◽  
Alakananda Hajra
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis

scholarly journals Stereoselective synthesis of chromane derivatives via a domino reaction catalyzed by modularly designed organocatalysts

2019 ◽  
Vol 17 (1) ◽  
pp. 151-155 ◽  
Author(s):  
Satish Jakkampudi ◽  
Ramarao Parella ◽  
John C.-G. Zhao
Keyword(s):  
Stereoselective Synthesis ◽  
Domino Reaction ◽  
Diastereoselective Synthesis

A highly enantio- and diastereoselective synthesis of functionalized chroman-2-ones and chromanes was achieved.

Functionalization of an sp3 C–H bond via a redox-neutral domino reaction: diastereoselective synthesis of hexahydropyrrolo[2,1-b]oxazoles

2014 ◽  
Vol 50 (22) ◽  
pp. 2951 ◽  
Author(s):  
Matiur Rahman ◽  
Avik Kumar Bagdi ◽  
Subhajit Mishra ◽  
Alakananda Hajra
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis

scholarly journals Diastereoselective Synthesis of Spiro[pyrazolone-4,3′-tetrahydrothiophenes] via a Sulfa-Michael/Aldol Domino Reaction

Synthesis ◽  
2016 ◽  
Vol 48 (23) ◽  
pp. 4091-4098 ◽  
Author(s):  
Dieter Enders ◽  
Uğur Kaya ◽  
Suruchi Mahajan ◽  
Jan-Hendrik Schöbel ◽  
Arto Valkonen ◽  
...  
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis

ChemInform Abstract: Diastereoselective Synthesis of Spirooxindole Derivatives via Biocatalytic Domino Reaction.

ChemInform ◽  
2015 ◽  
Vol 46 (21) ◽  
pp. no-no
Author(s):  
Yi-Ru Liang ◽  
Xiao-Yang Chen ◽  
Qi Wu ◽  
Xian-Fu Lin
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis

ChemInform Abstract: Diastereoselective Synthesis of 1,3-Diamines by a Domino Reaction of Imines, Enamines, and Trichlorosilane.

ChemInform ◽  
2014 ◽  
Vol 45 (35) ◽  
pp. no-no
Author(s):  
Takeru Kashiwagi ◽  
Shunsuke Kotani ◽  
Makoto Nakajima ◽  
Masaharu Sugiura
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis

Theophylline as the catalyst for the diastereoselective synthesis of trans-1,2-dihydrobenzo[a]furo[2,3-c]phenazines in water

RSC Advances ◽  
2016 ◽  
Vol 6 (87) ◽  
pp. 84326-84333 ◽  
Author(s):  
Afshin Yazdani-Elah-Abadi ◽  
Razieh Mohebat ◽  
Malek-Taher Maghsoodlou
Keyword(s):  
Environmentally Benign ◽  
Domino Reaction ◽  
Diastereoselective Synthesis ◽  
Reaction In Water ◽  
Pyridinium Ylide

Theophylline-catalyzed efficient and environmentally benign procedure for the diastereoselective synthesis of trans-1,2-dihydrobenzo[a]furo[2,3-c]phenazines with pyridinium ylide assisted domino reaction in water.

Indium(iii) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines

2015 ◽  
Vol 51 (4) ◽  
pp. 707-710 ◽  
Author(s):  
Sengodagounder Muthusamy ◽  
Manickasamy Sivaguru ◽  
Eringathodi Suresh
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis ◽  
Propargylic Alcohols

An atom-economical diastereoselective synthesis of indenodithiepines and indenodithiocines has been developed via a domino reaction of propargylic alcohols and dithioacetals in the presence of InCl3 as a catalyst.

A facile and highly diastereoselective synthesis of carbocyclic spiro-pyrazolones via DABCO catalyzed Michael-Michael domino reaction

Tetrahedron ◽  
2018 ◽  
Vol 74 (38) ◽  
pp. 5270-5279 ◽  
Author(s):  
Nirmal K. Rana ◽  
Khyati Shukla ◽  
Pratibha Mahto ◽  
Rupesh K. Jha ◽  
Vinod K. Singh
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis
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