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Refinado por: Nome da Publicação: Tetrahedron Letters remover
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1
Synthesis of biologically active natural products by [3+2] cycloaddition of non-stabilized azomethine ylides (AMY): Concepts and realizations
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Synthesis of biologically active natural products by [3+2] cycloaddition of non-stabilized azomethine ylides (AMY): Concepts and realizations

Pandey, Ganesh ; Dey, Debasis ; Tiwari, Sandip Kumar

Tetrahedron letters, 2017-02, Vol.58 (8), p.699-705 [Periódico revisado por pares]

Elsevier Ltd

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2
Recent topics of the natural product synthesis by Horner–Wadsworth–Emmons reaction
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Recent topics of the natural product synthesis by Horner–Wadsworth–Emmons reaction

Kobayashi, Kenichi ; Tanaka, Kosaku ; Kogen, Hiroshi

Tetrahedron letters, 2018-02, Vol.59 (7), p.568-582 [Periódico revisado por pares]

Elsevier Ltd

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3
Synthetic approach to seco-tetracenomycin natural products saccharothrixone A–C
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Synthetic approach to seco-tetracenomycin natural products saccharothrixone A–C

Chinta, Bhavani Shankar ; Sanapa, Harikrishna ; Vasikarla, Kamala Prasad ; Baire, Beeraiah

Tetrahedron letters, 2018-05, Vol.59 (20), p.1970-1973 [Periódico revisado por pares]

Elsevier Ltd

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4
Total synthesis of bioactive drimane–epoxyquinol hybrid natural products: macrophorin A, 4′-oxomacrophorin A, and 1′-epi-craterellin A
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Total synthesis of bioactive drimane–epoxyquinol hybrid natural products: macrophorin A, 4′-oxomacrophorin A, and 1′-epi-craterellin A

Garai, Sumanta ; Mehta, Goverdhan

Tetrahedron letters, 2014-11, Vol.55 (45), p.6252-6256 [Periódico revisado por pares]

Elsevier Ltd

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5
Recent topics in application of selective Rh(II)-catalyzed C H functionalization toward natural product synthesis
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Recent topics in application of selective Rh(II)-catalyzed C H functionalization toward natural product synthesis

Yakura, Takayuki ; Nambu, Hisanori

Tetrahedron letters, 2018-01, Vol.59 (3), p.188-202 [Periódico revisado por pares]

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6
Synthesis of tetrahydro-β-carbolines, β-carbolines, and natural products, (±)-harmicine, eudistomin U and canthine by reductive Pictet Spengler cyclization
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Artigo
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Synthesis of tetrahydro-β-carbolines, β-carbolines, and natural products, (±)-harmicine, eudistomin U and canthine by reductive Pictet Spengler cyclization

Pakhare, Deepali S. ; Kusurkar, Radhika S.

Tetrahedron letters, 2015-10, Vol.56 (44), p.6012-6015 [Periódico revisado por pares]

Elsevier Ltd

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7
A general, concise, ‘collective’ approach to eudesmanolide sesquiterpenoids: total synthesis of bioactive atractylenolides I–IV and related natural products
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A general, concise, ‘collective’ approach to eudesmanolide sesquiterpenoids: total synthesis of bioactive atractylenolides I–IV and related natural products

Ramesh, Subburethinam ; Mehta, Goverdhan

Tetrahedron letters, 2015-10, Vol.56 (41), p.5545-5548 [Periódico revisado por pares]

Elsevier Ltd

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8
Diels–Alder reaction of two green chiral precursors. Approach to natural product like structures
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Diels–Alder reaction of two green chiral precursors. Approach to natural product like structures

Carrau, Gonzalo ; Veiga, Nicolas ; Suescun, Leopoldo ; Giri, Germán F. ; Suárez, Alejandra G. ; Spanevello, Rolando ; González, David

Tetrahedron letters, 2016-10, Vol.57 (43), p.4791-4794 [Periódico revisado por pares]

Elsevier Ltd

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9
Enantioselective syntheses of bioactive epoxyquinone natural products (+)-harveynone and (−)-asperpentyn
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Enantioselective syntheses of bioactive epoxyquinone natural products (+)-harveynone and (−)-asperpentyn

Mehta, Goverdhan ; Roy, Subhrangsu ; Pan, Subhas Chandra

Tetrahedron letters, 2012-08, Vol.53 (32), p.4093-4095 [Periódico revisado por pares]

Elsevier Ltd

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10
First enantioselective total synthesis of (−)-dysibetaine CPa and absolute configurations of natural product
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First enantioselective total synthesis of (−)-dysibetaine CPa and absolute configurations of natural product

Sakai, Michihiro ; Ishikawa, Yuichi ; Takamizawa, Satoshi ; Oikawa, Masato

Tetrahedron letters, 2013-10, Vol.54 (44), p.5911-5912 [Periódico revisado por pares]

Elsevier Ltd

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