Academic literature on the topic 'CryptopyranmoscatoneB2'

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Journal articles on the topic "CryptopyranmoscatoneB2"

1

Maheswara Reddy, A., Gowravaram Sabitha, and Sirisha katukuri. "First total synthesis of cryptopyranmoscatone A2 from d-ribose." RSC Advances 5, no. 45 (2015): 35746–52. http://dx.doi.org/10.1039/c5ra03706a.

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2

Hu, Chao, Ziyang Zhao, Pengpeng Nie, Yuguo Du, Fu Feng, and Jun Liu. "Total synthesis of cryptopyranmoscatone B2." Tetrahedron 105 (January 2022): 132609. http://dx.doi.org/10.1016/j.tet.2021.132609.

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3

Reddy, A., and Gowravaram Sabitha. "First Total Synthesis of Cryptopyranmoscatone A3 and Crypto­pyranmoscatone B4." SynOpen 02, no. 01 (January 2018): 0058–63. http://dx.doi.org/10.1055/s-0036-1591931.

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The first total synthesis of cryptopyranmoscatones A3 and B4 has been accomplished from d-ribose or but-3-ynol. The key steps involved in the synthesis are oxa-Michael addition, highly diastereo­selective Brown allylation, and ring closing metathesis (RCM) and cross metathesis (CM) reactions.
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4

Sabitha, Gowravaram, S. Siva Sankara Reddy, and J. S. Yadav. "Stereoselective total synthesis of cryptopyranmoscatone A1." Tetrahedron Letters 52, no. 18 (May 2011): 2407–9. http://dx.doi.org/10.1016/j.tetlet.2011.02.107.

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5

Vaithegi, Kannan, and Kavirayani R. Prasad. "Enantiospecific total synthesis of the putative structure of cryptopyranmoscatone B2." Tetrahedron 74, no. 21 (May 2018): 2627–33. http://dx.doi.org/10.1016/j.tet.2018.04.011.

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6

Sabitha, Gowravaram, S. Siva Sankara Reddy, and J. S. Yadav. "Total synthesis of cryptopyranmoscatone B1 from 3,4,6-tri-O-acetyl-d-glucal." Tetrahedron Letters 51, no. 48 (December 2010): 6259–61. http://dx.doi.org/10.1016/j.tetlet.2010.09.085.

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7

Kundeti, Lakshmi Srinivasa Rao, Vijaya Vardhan Chinnam, Ambati Sharada, Akella Venkata Subrahmanya Sarma, Nagaiah Kommu, and Jhillu Singh Yadav. "Domino Intramolecular Ring‐Closing Metathesis/Cross‐Metathesis Reaction: Total Synthesis of Putative Structure of Cryptopyranmoscatone A2." ChemistrySelect 7, no. 44 (November 24, 2022). http://dx.doi.org/10.1002/slct.202202806.

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