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Refinado por: Nome da Publicação: Tetrahedron remover
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1
The Synthesis of 6-Azido and 6-Amino Analogues of 1-Deoxynojirimycin and their Conversion to Bicyclic Derivatives
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The Synthesis of 6-Azido and 6-Amino Analogues of 1-Deoxynojirimycin and their Conversion to Bicyclic Derivatives

Kilonda, Amuri ; Compernolle, Frans ; Peeters, Koen ; Joly, Gert J ; Toppet, Suzanne ; Hoornaert, Georges J

Tetrahedron, 2000-02, Vol.56 (7), p.1005-1012 [Periódico revisado por pares]

Elsevier Ltd

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2
Twisted molecular geometry and localized electronic structure of the triplet excited gem-diphenyltrimethylenemethane biradical: substituent effects on thermoluminescence and related theoretical calculations
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Twisted molecular geometry and localized electronic structure of the triplet excited gem-diphenyltrimethylenemethane biradical: substituent effects on thermoluminescence and related theoretical calculations

Matsui, Yasunori ; Namai, Hayato ; Akimoto, Ikuko ; Kan’no, Ken-ichi ; Mizuno, Kazuhiko ; Ikeda, Hiroshi

Tetrahedron, 2011-09, Vol.67 (38), p.7431-7439 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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3
Asymmetric synthesis of d-fagomine and its diastereoisomers
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Asymmetric synthesis of d-fagomine and its diastereoisomers

Davies, Stephen G. ; Fletcher, Ai M. ; Kennedy, Matthew S. ; Roberts, Paul M. ; Thomson, James E.

Tetrahedron, 2018-12, Vol.74 (51), p.7261-7271 [Periódico revisado por pares]

Elsevier Ltd

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4
Ketenimine mediated synthesis of lactam iminosugars: development of one-pot process via tandem hydrative amidation of amino-alkynes and intramolecular transamidation
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Ketenimine mediated synthesis of lactam iminosugars: development of one-pot process via tandem hydrative amidation of amino-alkynes and intramolecular transamidation

Arora, Inderpreet ; Shaw, Arun K.

Tetrahedron, 2016-09, Vol.72 (35), p.5479-5487 [Periódico revisado por pares]

Elsevier Ltd

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5
Synthesis and glycosidase inhibition properties of triazole-linked calixarene–iminosugar clusters
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Synthesis and glycosidase inhibition properties of triazole-linked calixarene–iminosugar clusters

Marra, Alberto ; Zelli, Renaud ; D'Orazio, Giuseppe ; La Ferla, Barbara ; Dondoni, Alessandro

Tetrahedron, 2014-12, Vol.70 (49), p.9387-9393 [Periódico revisado por pares]

Elsevier Ltd

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6
α- and β-Glucosidase inhibitors: chemical structure and biological activity
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α- and β-Glucosidase inhibitors: chemical structure and biological activity

Borges de Melo, Eduardo ; da Silveira Gomes, Adriane ; Carvalho, Ivone

Tetrahedron, 2006-10, Vol.62 (44), p.10277-10302 [Periódico revisado por pares]

Elsevier Ltd

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7
Asymmetric syntheses of fagomine and its stereoisomers
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Asymmetric syntheses of fagomine and its stereoisomers

Davies, Stephen G. ; Fletcher, Ai M. ; Roberts, Paul M. ; Thomson, James E.

Tetrahedron, 2019-12, Vol.75 (50), p.130727, Article 130727 [Periódico revisado por pares]

Elsevier Ltd

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8
Efficient and stereoselective syntheses of DAB-1 and d-fagomine via chiral 1,3-oxazine
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Efficient and stereoselective syntheses of DAB-1 and d-fagomine via chiral 1,3-oxazine

Kim, Ji-Yeon ; Mu, Yu ; Jin, Xiangdan ; Park, Seok-Hwi ; Pham, Van-Thoai ; Song, Dong-Keun ; Lee, Kee-Young ; Ham, Won-Hun

Tetrahedron, 2011-12, Vol.67 (48), p.9426-9432 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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9
Morusalbanol A, a neuro-protective Diels–Alder adduct with an unprecedented architecture from Morus alba
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Morusalbanol A, a neuro-protective Diels–Alder adduct with an unprecedented architecture from Morus alba

Chen, Hua-Dong ; Ding, Yuan-Qing ; Yang, Sheng-Ping ; Li, Xing-Cong ; Wang, Xu-Jie ; Zhang, Hai-Yan ; Ferreira, Daneel ; Yue, Jian-Min

Tetrahedron, 2012-07, Vol.68 (30), p.6054-6058 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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10
Highly stereoselective synthesis of imino-C-di- and trisaccharides as hydrolytically stable glycomimetics
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Highly stereoselective synthesis of imino-C-di- and trisaccharides as hydrolytically stable glycomimetics

Marca, Eduardo ; Delso, Ignacio ; Tejero, Tomás ; Merino, Pedro

Tetrahedron, 2012-08, Vol.68 (33), p.6674-6687 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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