Relevant bibliographies by topics / Cleistenolide

Academic literature on the topic 'Cleistenolide'

Author: Grafiati
Published: 6 September 2023

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Journal articles on the topic "Cleistenolide"

1

Schmidt, Bernd, Oliver Kunz, and Anne Biernat. "Total Synthesis of (−)-Cleistenolide." Journal of Organic Chemistry 75, no. 7 (April 2, 2010): 2389–94. http://dx.doi.org/10.1021/jo1002642.

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2

Ramesh, Palakuri, and H. M. Meshram. "Total synthesis of (−)-cleistenolide." Tetrahedron Letters 52, no. 19 (May 2011): 2443–45. http://dx.doi.org/10.1016/j.tetlet.2011.01.124.

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3

Chanti Babu, Dokuburra, Kankati Ashalatha, Chitturi Bhujanga Rao, Jon Paul Selvam Jondoss, and Yenamandra Venkateswarlu. "Total Synthesis of (−)-Cleistenolide." Helvetica Chimica Acta 94, no. 12 (December 2011): 2215–20. http://dx.doi.org/10.1002/hlca.201100086.

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4

Samwel, Stephen, Stephen J. M. Mdachi, Mayunga H. H. Nkunya, Beatrice N. Irungu, Mainen J. Moshi, Brian Moulton, and Brian S. Luisi. "Cleistenolide and Cleistodienol: Novel Bioactive Constituents of Cleistochlamys kirkii." Natural Product Communications 2, no. 7 (July 2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200706.

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Abstract:
(-)-5-Acetoxy-6-(1-benzoyloxy-2-acetoxyethyl)-pyr-3-en-2-one (cleistenolide) and (-)-2,6-diacetoxy-5-hydroxy-cyclohex-3-enylidenemethyl benzoate (cleistodienol) were isolated as novel antimicrobial and cytotoxic constituents of Cleistochlamys kirkii (Annonaceae), together with ( Z)-(+)-5-(2,3-dihydroxy-propylidene)-5 H-furan-2-one and its acetyl and benzoyl derivatives, (-)-1,6-desoxy-β-senepoxide, pinocembrin and polycarpol. Structural determination was achieved based on spectroscopic and other physical data. The structure of cleistenolide was confirmed by single crystal X-ray crystallographic analysis.
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5

Cai, Chao, Jun Liu, Yuguo Du, and Robert J. Linhardt. "Stereoselective Total Synthesis of (−)-Cleistenolide." Journal of Organic Chemistry 75, no. 16 (August 20, 2010): 5754–56. http://dx.doi.org/10.1021/jo101059e.

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6

Chanti Babu, Dokuburra, Jondoss Jon Paul Selavam, Dorigondla Kumar Reddy, Vanam Shekhar, and Yenamandra Venkateswarlu. "Stereoselective total synthesis of (−)-cleistenolide." Tetrahedron 67, no. 21 (May 2011): 3815–19. http://dx.doi.org/10.1016/j.tet.2011.03.107.

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7

Subba Reddy, B. V., B. Phaneendra Reddy, T. Pandurangam, and J. S. Yadav. "The stereoselective total synthesis of (−)-cleistenolide." Tetrahedron Letters 52, no. 18 (May 2011): 2306–8. http://dx.doi.org/10.1016/j.tetlet.2011.02.025.

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8

Reddy, A. Bal, B. Kumara Swamy, and Jhillu Singh Yadav. "A concise total synthesis of cleistenolide." Tetrahedron: Asymmetry 27, no. 16 (September 2016): 788–90. http://dx.doi.org/10.1016/j.tetasy.2016.06.012.

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9

Mahajan, Pankaj S., Rajesh G. Gonnade, and Santosh B. Mhaske. "Protecting-Group-Free Diastereoselective Total Synthesis of (±)-6-epi-Cleistenolide and Chemoenzymatic Synthesis of (-)-6-epi-Cleistenolide." European Journal of Organic Chemistry 2014, no. 36 (October 31, 2014): 8049–54. http://dx.doi.org/10.1002/ejoc.201403123.

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10

Vijaya Kumar, T., K. Suresh Babu, and J. Madhusudana Rao. "A simple and efficient stereoselective synthesis of (−)-cleistenolide." Tetrahedron Letters 53, no. 14 (April 2012): 1823–25. http://dx.doi.org/10.1016/j.tetlet.2012.01.123.

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