Log in

Relevant bibliographies by topics / Diospongin / Journal articles

To see the other types of publications on this topic, follow the link: Diospongin.

Journal articles on the topic 'Diospongin'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 48 journal articles for your research on the topic 'Diospongin.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Bates, Roderick W., and Ping Song. "Synthesis of diospongin A." Tetrahedron 63, no. 21 (2007): 4497–99. http://dx.doi.org/10.1016/j.tet.2007.03.058.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Zúñiga, Andrea, Manuel Pérez, Zoila Gándara, Alioune Fall, Generosa Gómez, and Yagamare Fall. "Synthesis of diospongin A, ent-diospongin A and C-5 epimer of diospongin B from tri-O-acetyl-D-glucal." Arkivoc 2015, no. 7 (2015): 195–215. http://dx.doi.org/10.3998/ark.5550190.p009.191.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Vaithegi, Kannan, and Kavirayani R. Prasad. "Total synthesis of (+)-diospongin A." Tetrahedron 76, no. 47 (2020): 131625. http://dx.doi.org/10.1016/j.tet.2020.131625.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Bharath, Yada, Utkal Mani Choudhury, N. Sadhana, and Debendra K. Mohapatra. "The Mukaiyama type aldol reaction for the synthesis of trans-2,6-disubstituted tetrahydropyrans: synthesis of diospongin A and B." Organic & Biomolecular Chemistry 17, no. 41 (2019): 9169–81. http://dx.doi.org/10.1039/c9ob01549c.

Full text

Abstract:

The synthesis of 2,6-trans-disubstituted tetrahydropyrans following the Mukaiyama type aldol reaction through C–C bond formation demonstrates the practicality of this protocol in the total synthesis of diospongin A and B.

APA, Harvard, Vancouver, ISO, and other styles

5

Chandrasekhar, S., T. Shyamsunder, S. Jaya Prakash, A. Prabhakar, and B. Jagadeesh. "First total synthesis of (−)-diospongin B." Tetrahedron Letters 47, no. 1 (2006): 47–49. http://dx.doi.org/10.1016/j.tetlet.2005.10.129.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Meruva, Suresh Babu, Ramamohan Mekala, Akula Raghunadh, et al. "Synthesis of tetrahedral diarylheptanoid ent-diospongin A and epimer-diospongin B by employing Julia–Kocienski olefination." Tetrahedron Letters 55, no. 34 (2014): 4739–41. http://dx.doi.org/10.1016/j.tetlet.2014.06.112.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Hiebel, Marie-Aude, Béatrice Pelotier, and Olivier Piva. "Total synthesis of (+/−)-diospongin A via Prins reaction." Tetrahedron 63, no. 33 (2007): 7874–78. http://dx.doi.org/10.1016/j.tet.2007.05.089.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Cossy, Janine, Cyril Bressy, and Florent Allais. "A Short and Efficient Synthesis of (-)-Diospongin A." Synlett 2006, no. 20 (2006): 3455–56. http://dx.doi.org/10.1055/s-2006-956485.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Ho, Tse-Lok, Bin Tang, Guohua Ma, and Pengfei Xu. "Concise Synthesis of Yashabushidiol A and (±)-Diospongin A." Journal of the Chinese Chemical Society 59, no. 3 (2012): 455–58. http://dx.doi.org/10.1002/jccs.201100664.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Meruva, Suresh Babu, Ramamohan Mekala, Akula Raghunadh, et al. "ChemInform Abstract: Synthesis of Tetrahedral Diarylheptanoid ent-Diospongin A (I) and epimer-Diospongin B (II) by Employing Julia-Kocienski Olefination." ChemInform 46, no. 5 (2015): no. http://dx.doi.org/10.1002/chin.201505215.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Reddy, Chada Raji, Guvvala Balakrishna Reddy, and Boinapally Srikanth. "Stereoselective synthesis of a tetrahydropyranyl diarylheptanoid, ent-diospongin A." Tetrahedron: Asymmetry 22, no. 18-19 (2011): 1725–28. http://dx.doi.org/10.1016/j.tetasy.2011.10.006.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Chandrasekhar, S., G. S. Kiran Babu, and Ch Raji Reddy. "Asymmetric synthesis of aza-diospongin A as an iNOS inducer." Tetrahedron: Asymmetry 20, no. 19 (2009): 2216–19. http://dx.doi.org/10.1016/j.tetasy.2009.09.013.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Kumar, Rayala Naveen, and H. M. Meshram. "Total synthesis of (−)-diospongin A and (+)-cryptofolione via asymmetric aldol reaction." Tetrahedron Letters 52, no. 9 (2011): 1003–7. http://dx.doi.org/10.1016/j.tetlet.2010.12.070.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

More, Jesse. "Synthesis of (±)-Diospongin A: A Hetero-Diels-Alder and C-Glycosylation Approach." Synthesis 2010, no. 14 (2010): 2419–23. http://dx.doi.org/10.1055/s-0029-1218784.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

More, Jesse D. "ChemInform Abstract: Synthesis of (.+-.)-Diospongin A: A Hetero-Diels-Alder and C-Glycosylation Approach." ChemInform 41, no. 48 (2010): no. http://dx.doi.org/10.1002/chin.201048209.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Yadav, J., B. Padmavani, B. V. Reddy, Ch Venugopal, and A. Rao. "Total Synthesis of Diospongin A via an Enzymatic Kinetic Resolution of (±)-Tetrahydropyranol Derived from Prins Cyclization." Synlett 2007, no. 13 (2007): 2045–48. http://dx.doi.org/10.1055/s-2007-984886.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Karlubíková, Ol'ga, Matej Babjak, and Tibor Gracza. "Tetrahydropyran synthesis by palladium(II)-catalysed hydroxycarbonylation of hexenols: synthesis of (±)-diospongin A and (+)-civet cat compound." Tetrahedron 67, no. 27-28 (2011): 4980–87. http://dx.doi.org/10.1016/j.tet.2011.04.045.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Gharpure, Santosh J., Sumit P. Mane, Laxmi Narayan Nanda, and Manoj Kumar Shukla. "Stereoselective Synthesis of Donor-Acceptor Cyclopropapyranone by Intramolecular Cyclopropanation of Vinylogous Carbonates: Application to the Total Synthesis of (±)-Diospongin B." Israel Journal of Chemistry 56, no. 6-7 (2016): 553–57. http://dx.doi.org/10.1002/ijch.201500088.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Tong, Rongbiao, and Zhilong Li. "Asymmetric Total Syntheses of the trans-2-Aryl-6-alkyltetrahydropyrans Diospongin B and Parvistones D and E from a Common Precursor." Synthesis 48, no. 11 (2016): 1630–36. http://dx.doi.org/10.1055/s-0035-1561592.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Rybak, Taras, and Dennis G. Hall. "Stereoselective and Regiodivergent Allylic Suzuki–Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B." Organic Letters 17, no. 17 (2015): 4156–59. http://dx.doi.org/10.1021/acs.orglett.5b01906.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Rybak, Taras, and Dennis G. Hall. "ChemInform Abstract: Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B." ChemInform 47, no. 4 (2016): no. http://dx.doi.org/10.1002/chin.201604130.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Clarke, Paul A., Nadiah Mad Nasir, Philip B. Sellars, Alejandra M. Peter, Connor A. Lawson, and James L. Burroughs. "Synthesis of 2,6-trans- and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland–Japp derived 2H-dihydropyran-4-ones: a total synthesis of diospongin B." Organic & Biomolecular Chemistry 14, no. 28 (2016): 6840–52. http://dx.doi.org/10.1039/c6ob01182a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Kumaraswamy, Gullapalli, and Dasa Rambabu. "A flexible enantioselective synthesis of (+)-centrolobine and 5-epi-diospongin-A using asymmetric transfer hydrogenation/tandem Grubbs cross-metathesis/oxy-Michael reaction as key steps." Tetrahedron: Asymmetry 24, no. 4 (2013): 196–201. http://dx.doi.org/10.1016/j.tetasy.2013.01.005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Lee, Kiyoun, Hyoungsu Kim, and Jiyong Hong. "A Facile and Efficient Synthesis of 4-Hydroxy-2,6-cis-tetrahydropyrans via Tandem Cross-Metathesis/Thermal SN2′ Reaction: Protecting-Group-Free Synthesis of (±)-Diospongin A." Organic Letters 11, no. 22 (2009): 5202–5. http://dx.doi.org/10.1021/ol902125d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Yao, Hongliang, Jingyun Ren, and Rongbiao Tong. "A short and flexible route to tetrahydropyran-4-ones via conjugated nitrile oxidescycloaddition and oxa-Michael cyclization: a concise diastereoselective total synthesis of (±)-diospongin A." Chem. Commun. 49, no. 2 (2013): 193–95. http://dx.doi.org/10.1039/c2cc37772a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Yao, Hongliang, Jingyun Ren, and Rongbiao Tong. "ChemInform Abstract: A Short and Flexible Route to Tetrahydropyran-4-ones via Conjugated Nitrile Oxides Cycloaddition and Oxa-Michael Cyclization: A Concise Diastereoselective Total Synthesis of (.+-.)-Diospongin A." ChemInform 44, no. 20 (2013): no. http://dx.doi.org/10.1002/chin.201320153.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Xian, Ming, Hua Wang, and Brian Shuhler. "Total Syntheses of Diospongins A and B." Synlett 2008, no. 17 (2008): 2651–54. http://dx.doi.org/10.1055/s-0028-1083518.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Stefan, Eric, Ansel P. Nalin, and Richard E. Taylor. "Concise enantioselective synthesis of diospongins A and B." Tetrahedron 69, no. 36 (2013): 7706–12. http://dx.doi.org/10.1016/j.tet.2013.05.081.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Sabitha, Gowravaram, Pannala Padmaja, and Jhillu S Yadav. "A Concise Total Synthesis of Diospongins A and B." Helvetica Chimica Acta 91, no. 12 (2008): 2235–39. http://dx.doi.org/10.1002/hlca.200890242.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Kawai, Nobuyuki, Sudhir Mahadeo Hande, and Jun'ichi Uenishi. "Stereoselective synthesis of (−)-diospongins A and B and their stereoisomers at C-5." Tetrahedron 63, no. 37 (2007): 9049–56. http://dx.doi.org/10.1016/j.tet.2007.06.081.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Sawant, Kailas B., та Michael P. Jennings. "Efficient Total Syntheses and Structural Verification of Both Diospongins A and B via a Common δ-Lactone Intermediate". Journal of Organic Chemistry 71, № 20 (2006): 7911–14. http://dx.doi.org/10.1021/jo061296f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Piva, Olivier, Ludovic Raffier, and Frédéric Izquierdo. "Desymmetrization of Hepta-1,6-dien-4-ol by Prins Reaction and Subsequent Cross-Metathesis: Access to Diospongine A Homologues." Synthesis 2011, no. 24 (2011): 4037–44. http://dx.doi.org/10.1055/s-0031-1289588.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Anada, Masahiro, Takuya Washio, Yudai Watanabe, Koji Takeda, and Shunichi Hashimoto. "A Short, Catalytic, Asymmetric Synthesis of Diospongins A and B by a One-Pot, Sequential Hetero-Diels-Alder/Mukaiyama-Michael Reaction Process." European Journal of Organic Chemistry 2010, no. 35 (2010): 6850–54. http://dx.doi.org/10.1002/ejoc.201001125.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Kumaraswamy, Gullapalli, Gajula Ramakrishna, Police Naresh, Bharatam Jagadeesh, and Balasubramanian Sridhar. "A Flexible Enantioselective Total Synthesis of Diospongins A and B and Their Enantiomers Using Catalytic Hetero-Diels−Alder/Rh-Catalyzed 1,4-Addition and Asymmetric Transfer Hydrogenation Reactions as Key Steps." Journal of Organic Chemistry 74, no. 21 (2009): 8468–71. http://dx.doi.org/10.1021/jo901739y.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Bates, Roderick W., and Ping Song. "Synthesis of Diospongin A." ChemInform 38, no. 35 (2007). http://dx.doi.org/10.1002/chin.200735215.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Chandrasekhar, S., T. Shyamsunder, S. Jaya Prakash, A. Prabhakar, and B. Jagadeesh. "First Total Synthesis of (-)-Diospongin B." ChemInform 37, no. 18 (2006). http://dx.doi.org/10.1002/chin.200618220.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Bressy, Cyril, Florent Allais, and Janine Cossy. "A Short and Efficient Synthesis of (-)-Diospongin A." ChemInform 38, no. 17 (2007). http://dx.doi.org/10.1002/chin.200717197.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Hiebel, Marie-Aude, Beatrice Pelotier, and Olivier Piva. "Total Synthesis of (+/-)-Diospongin A via Prins Reaction." ChemInform 38, no. 47 (2007). http://dx.doi.org/10.1002/chin.200747205.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Jun, Yin, Liu Zhihui, Han Na, and Xiao Bin. "Relative and Absolute Structures of Diospongin A, B and C." Planta Medica 75, no. 04 (2009). http://dx.doi.org/10.1055/s-2009-1216410.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Chandrasekhar, S., G. S. Kiran Babu, and Ch Raji Reddy. "ChemInform Abstract: Asymmetric Synthesis of aza-Diospongin as an iNOS Inducer." ChemInform 41, no. 12 (2010). http://dx.doi.org/10.1002/chin.201012194.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Yadav, J. S., B. Padmavani, B. V. Subba Reddy, Ch Venugopal, and A. Bhaskar Rao. "ChemInform Abstract: Total Synthesis of Diospongin A via an Enzymatic Kinetic Resolution of (.+-.)-Tetrahydropyranol Derived from Prins Cyclization." ChemInform 39, no. 1 (2008). http://dx.doi.org/10.1002/chin.200801218.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Gharpure, Santosh J., Sumit P. Mane, Laxmi Narayan Nanda, and Manoj Kumar Shukla. "ChemInform Abstract: Stereoselective Synthesis of Donor-Acceptor Cyclopropapyranone by Intramolecular Cyclopropanation of Vinylogous Carbonates: Application to the Total Synthesis of (.+-.)-Diospongin B." ChemInform 47, no. 47 (2016). http://dx.doi.org/10.1002/chin.201647152.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Li, Zhilong, and Rongbiao Tong. "ChemInform Abstract: Asymmetric Total Syntheses of the trans-2-Aryl-6-alkyltetrahydropyrans Diospongin B and Parvistones D and E from a Common Precursor." ChemInform 47, no. 43 (2016). http://dx.doi.org/10.1002/chin.201643180.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Clarke, Paul A., Nadiah Mad Nasir, Philip B. Sellars, Alejandra M. Peter, Connor A. Lawson, and James L. Burroughs. "ChemInform Abstract: Synthesis of 2,6-trans- and 3,3,6-Trisubstituted Tetrahydropyran-4-ones from Maitland-Japp Derived 2H-Dihydropyran-4-ones: A Total Synthesis of Diospongin B." ChemInform 47, no. 49 (2016). http://dx.doi.org/10.1002/chin.201649147.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Sabitha, Gowravaram, Pannala Padmaja, and Jhillu S. Yadav. "ChemInform Abstract: A Concise Total Synthesis of Diospongins A (VII) and B (VIII)." ChemInform 40, no. 18 (2009). http://dx.doi.org/10.1002/chin.200918195.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Kawai, Nobuyuki, Sudhir Mahadeo Hande, and Jun'ichi Uenishi. "ChemInform Abstract: Stereoselective Synthesis of (-)-Diospongins A and B and Their Stereoisomers at C-5." ChemInform 39, no. 4 (2008). http://dx.doi.org/10.1002/chin.200804221.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Sawant, Kailas B., та Michael P. Jennings. "Efficient Total Syntheses and Structural Verification of Both Diospongins A (IIa) and B (IIb) via a Common δ-Lactone Intermediate (I)." ChemInform 38, № 6 (2007). http://dx.doi.org/10.1002/chin.200706195.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Kumaraswamy, Gullapalli, Gajula Ramakrishna, Police Naresh, Bharatam Jagadeesh, and Balasubramanian Sridhar. "ChemInform Abstract: A Flexible Enantioselective Total Synthesis of Diospongins A (I) and B (II) and Their Enantiomers Using Catalytic Hetero-Diels-Alder/Rh-Catalyzed 1,4-Addition and Asymmetric Transfer Hydrogenation Reactions as Key Steps." ChemInform 41, no. 12 (2010). http://dx.doi.org/10.1002/chin.201012196.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!