Relevant bibliographies by topics / Cardiobutanolide

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Cardiobutanolide'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 September 2023

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Journal articles on the topic "Cardiobutanolide"

1

Garg, Ashish, Ravi P. Singh, and Vinod K. Singh. "Asymmetric synthesis of (+)-cardiobutanolide." Tetrahedron 62, no. 48 (2006): 11240–44. http://dx.doi.org/10.1016/j.tet.2006.09.005.

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Radha Krishna, Palakodety, and P. V. Narsimha Reddy. "Stereoselective total synthesis of (+)-cardiobutanolide and (+)-3-epi-cardiobutanolide from diacetone d-glucose." Tetrahedron Letters 47, no. 27 (2006): 4627–30. http://dx.doi.org/10.1016/j.tetlet.2006.04.146.

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3

Prasad, Kavirayani R., and Shivajirao L. Gholap. "Stereoselective Total Synthesis of (+)-Cardiobutanolide." Journal of Organic Chemistry 73, no. 7 (2008): 2916–19. http://dx.doi.org/10.1021/jo7025614.

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Krishna, Palakodety Radha, and P. V. Narsimha Reddy. "Corrigendum to “Stereoselective total synthesis of (+)-cardiobutanolide and (+)-3-epi-cardiobutanolide from diacetone d-glucose”." Tetrahedron Letters 47, no. 37 (2006): 6695. http://dx.doi.org/10.1016/j.tetlet.2006.06.093.

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5

Hisham, A., M. Toubi, W. Shuaily, M. D. Ajitha Bai, and Y. Fujimoto. "Cardiobutanolide, a styryllactone from Goniothalamus cardiopetalus." Phytochemistry 62, no. 4 (2003): 597–600. http://dx.doi.org/10.1016/s0031-9422(02)00536-8.

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6

Yadav, J., B. Madhavarao, and K. Rao. "Total Synthesis of (+)-Cardiobutanolide through a Carbohydrate-Based Approach." Synlett 2009, no. 19 (2009): 3179–81. http://dx.doi.org/10.1055/s-0029-1218344.

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7

Ruiz, Purificación, Juan Murga, Miguel Carda, and J. Alberto Marco. "Stereoselective Synthesis of the Naturally Occurring Styryllactones (+)-Goniofufurone and (+)-Cardiobutanolide." Journal of Organic Chemistry 70, no. 2 (2005): 713–16. http://dx.doi.org/10.1021/jo0483116.

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8

Fernandes, Rodney A., and Pullaiah Kattanguru. "Step-Economic and Protecting-Group-Free Total Synthesis of (+)-Cardiobutanolide." Asian Journal of Organic Chemistry 2, no. 1 (2012): 74–84. http://dx.doi.org/10.1002/ajoc.201200130.

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Kovačević, Ivana, Mirjana Popsavin, Marko V. Rodić, Vesna Kojić, and Velimir Popsavin. "Asymmetric synthesis of the cytotoxic lactone (+)-cardiobutanolide and two novel analogues." Tetrahedron Letters 60, no. 9 (2019): 684–87. http://dx.doi.org/10.1016/j.tetlet.2019.01.059.

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10

Chandrasekhar, S., and N. Kiranmai. "Asymmetric total synthesis of (+)-cardiobutanolide via an iterative asymmetric dihydroxylation in PEG." Tetrahedron Letters 51, no. 31 (2010): 4058–60. http://dx.doi.org/10.1016/j.tetlet.2010.05.122.

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Dissertations / Theses on the topic "Cardiobutanolide"

1

Wang, Jun. "Towards protecting-group-free total synthesis cardiobutanolide in water." Thesis, McGill University, 2010. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=92361.

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A green stereoselective total synthesis of cardiobutanolide is proposed, starting from 1,6-dibromohexa-2,4-diene. The synthetic route consists of only 7 steps in total, where each step is performed in aqueous media, and no protecting groups are used. One of the key steps in the synthesis involves a combination of cyanide substitution and intramolecular Pinner reaction in one pot. Studies dealing with reaction process monitoring, tests of catalysts, and condition optimization are reported. A "no purification" process for the sequence of the first four steps of the synthesis is described.
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2

Bojana, Srećo Zelenović. "Dizajn, sinteza i antiproliferativna aktivnost prirodnih citotoksičnih laktona i analoga." Phd thesis, Univerzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, 2013. https://www.cris.uns.ac.rs/record.jsf?recordId=83673&source=NDLTD&language=en.

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Ostvarene su vi&scaron;efazne sinteze prirodnih citotoksičnih laktona (+)-murikatacina (<strong>1</strong>),(&ndash;)-murikatacina (ent-<strong>1</strong>) i (+)-goniofufurona (<strong>2</strong>), kao i njihovih novih analoga (<strong>3a</strong>,&nbsp; <strong>4</strong>,<strong>5</strong>,&nbsp; <strong>6</strong>,&nbsp; <strong>7</strong>,&nbsp; <strong>8</strong>,&nbsp; <strong>9</strong>,&nbsp; ent-<strong>7&nbsp;</strong>i ent-<strong>9</strong>), polazeći iz&nbsp; D-ksiloze ili iz&nbsp; D-glukoze. Ispitana je&nbsp; in vitrocitotoksična aktivnost sintetizovanih prirodnih proizvoda i ana
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3

Ivana, Kovačević. "Prirodni stiril-laktoni, njihovi derivati i analozi kao potencijalni antitumorski agensi: Dizajn, sinteza i SAR ispitivanja." Phd thesis, Univerzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, 2015. https://www.cris.uns.ac.rs/record.jsf?recordId=94214&source=NDLTD&language=en.

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U radu je ostvarena sinteza četiri prirodna proizvoda, goniobutenolida A i B,krasalaktona D i 3-deoksi-kardiobutanolida i 32 derivata i analoga polazeći izD-glukoze. Sinteza prirodnog stiril-laktona, kardiobutanolida&nbsp; i njegova 4derivata je izvedena polazeći iz&nbsp; D-ksiloze.&nbsp; Ispitan je uticaj sintetizovanihjedinjenja&nbsp; na inhibiciju rasta 10 tumorskih i jedne zdrave ćelijske linije.Uspostavljene su i&nbsp; korelacije izmedju strukture i antiproliferativne aktivnosti&nbsp;(SAR) i ispitan je mehanzam antitumorskog dejstva.<br>Synthesis of four natural products: goniobutenolide
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4

Wang, Jun. "Towards protecting-group-free total synthesis cardiobutanolide in water." 2008. http://digitool.Library.McGill.CA:8881/R/?func=dbin-jump-full&object_id=92361.

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5

Gholap, Shivajirao Lahu. "Steroselective Synthesis Of Bio-Active Styryllactones." Thesis, 2008. https://etd.iisc.ac.in/handle/2005/813.

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The thesis titled “Stereoselective synthesis of bio-active styryllactones” comprises an introduction about styryllactones and three sections delineating the results and discussion about the synthesis of styryllactones and experimental section. Trees of the genus Goniothalamus of the plant family Annonaceae in South East Asia has been known for a long time for their proven use in folk medicine. The research group of McLaughlin isolated and characterized a series of styryllactones, possessing significant to marginal cytotoxic activity against human tumor cell lines. The structures and relative
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Gholap, Shivajirao Lahu. "Steroselective Synthesis Of Bio-Active Styryllactones." Thesis, 2008. http://hdl.handle.net/2005/813.

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The thesis titled “Stereoselective synthesis of bio-active styryllactones” comprises an introduction about styryllactones and three sections delineating the results and discussion about the synthesis of styryllactones and experimental section. Trees of the genus Goniothalamus of the plant family Annonaceae in South East Asia has been known for a long time for their proven use in folk medicine. The research group of McLaughlin isolated and characterized a series of styryllactones, possessing significant to marginal cytotoxic activity against human tumor cell lines. The structures and relative
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