Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D

Dattatraya H. Dethe; Balu D. Dherange; Saghir Ali; Mahesh M. Parsutkar

doi:10.1039/c6ob02322c

Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D

Dattatraya H. Dethe, Balu D. Dherange, Saghir Ali, Mahesh M. Parsutkar

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Abstract

Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond formation reaction.

Original language	English (US)
Pages (from-to)	65-68
Number of pages	4
Journal	Organic and Biomolecular Chemistry
Volume	15
Issue number	1
DOIs	https://doi.org/10.1039/c6ob02322c
State	Published - 2017
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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abstract = "Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond formation reaction.",

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AU - Dethe, Dattatraya H.

AU - Dherange, Balu D.

AU - Ali, Saghir

AU - Parsutkar, Mahesh M.

N1 - Publisher Copyright: © The Royal Society of Chemistry.

PY - 2017

Y1 - 2017

N2 - Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond formation reaction.

AB - Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond formation reaction.

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U2 - 10.1039/c6ob02322c

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Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D

Abstract

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