Stereoselective total synthesis of diplodialide A-Reference-Cited by-同舟云学术

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Stereoselective total synthesis of diplodialide A

Published:2020-09-22 Issue:3 Volume:75 Page:931-937
ISSN:2585-7290
Container-title:Chemical Papers
language:en
Short-container-title:Chem. Pap.

Author:

Ramakrishna Kolluri,Sreenivasulu Reddymasu,Rao Mandava Venkata Basaveswara,Vidavalur Siddaiah,Reddy Boggu Jagan Mohan

Publisher

Springer Science and Business Media LLC

Subject

Materials Chemistry,Industrial and Manufacturing Engineering,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s11696-020-01365-1.pdf

Reference19 articles.

1. Anand RV, Baktharaman S, Singh VK (2003) A ring-closing metathesis approach toward formal total synthesis of (+)—Diplodialide A. J Org Chem 68:3356–3359. https://doi.org/10.1021/jo034049+

2. Boeckman RK, Pruitt JR (1989) A new, highly efficient, selective methodology for formation of medium-ring and macrocyclic lactones via intramolecular ketene trapping: an application to a convergent synthesis of (-)-Kromycin. J Am Chem Soc 111:8286–8288. https://doi.org/10.1021/ja00203a044

3. Drager G, Kirschning A, Thiericke R, Zerlin M (1996) Decanolides, 10 membered lactones of natural origin. Nat Prod Rep 13:365–375. https://doi.org/10.1039/NP9961300365

4. Ferraz MC, Bombonato FI, Longo LS (2007) Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis 21:3261–3285. https://doi.org/10.1055/s-2007-990831

5. Inanaga J, Hirata K, Saeki H, Katsuki T, Yamaguchi M (1979) A Rapid esterification by means of mixed anhydride and its application to large-ring lactonization. Bull Chem Soc Jpn 52:1989–1993. https://doi.org/10.1246/bcsj.52.1989

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