Tandem [1,2]-Wittig Rearrangement/Lactonization of γ-Benzyloxy Vinylogous Urethanes: Application to the Synthetic Studies of Maculalactone A, Planchol C and γ-Lycorane

Guo-Ming Ho; Yu-Jang Li

doi:10.1002/ajoc.201700589

Tandem [1,2]-Wittig Rearrangement/Lactonization of γ-Benzyloxy Vinylogous Urethanes: Application to the Synthetic Studies of Maculalactone A, Planchol C and γ-Lycorane

Asian Journal of Organic Chemistry ◽

10.1002/ajoc.201700589 ◽

2017 ◽

Vol 7 (1) ◽

pp. 145-149 ◽

Cited By ~ 2

Author(s):

Guo-Ming Ho ◽

Yu-Jang Li

Keyword(s):

Wittig Rearrangement ◽

Synthetic Studies

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Synthetic studies of the nargenicins. Introduction of the C14-C19 side chain by diastereoselective [2,3] Wittig rearrangement of a tertiary allylic ether

The Journal of Organic Chemistry ◽

10.1021/jo00256a065 ◽

1988 ◽

Vol 53 (21) ◽

pp. 5189-5191 ◽

Cited By ~ 24

Author(s):

Lucius T. Rossano ◽

Daniel J. Plata ◽

James Kallmerten

Keyword(s):

Side Chain ◽

Wittig Rearrangement ◽

Synthetic Studies

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Cover Feature: Tandem [1,2]-Wittig Rearrangement/Lactonization of γ-Benzyloxy Vinylogous Urethanes: Application to the Synthetic Studies of Maculalactone A, Planchol C and γ-Lycorane (Asian J. Org. Chem. 1/2018)

Asian Journal of Organic Chemistry ◽

10.1002/ajoc.201700635 ◽

2018 ◽

Vol 7 (1) ◽

pp. 3-3

Author(s):

Guo-Ming Ho ◽

Yu-Jang Li

Keyword(s):

Wittig Rearrangement ◽

Synthetic Studies

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Synthetic Studies on CP-225,917 and CP-263,114: Access to Advanced Tetracyclic Systems by Intramolecular Conjugate Displacement and [2,3]-Wittig Rearrangement

The Journal of Organic Chemistry ◽

10.1021/jo302467w ◽

2013 ◽

Vol 78 (3) ◽

pp. 996-1013 ◽

Cited By ~ 18

Author(s):

Farzad Malihi ◽

Derrick L. J. Clive ◽

Che-Chien Chang ◽

Minaruzzaman

Keyword(s):

Wittig Rearrangement ◽

Intramolecular Conjugate Displacement ◽

Synthetic Studies

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Synthetic studies toward inducamide C

Organic & Biomolecular Chemistry ◽

10.1039/d0ob01995j ◽

2021 ◽

Author(s):

Ardalan A. Nabi ◽

Lydia M. Scott ◽

Daniel P. Furkert ◽

Jonathan Sperry

Keyword(s):

Natural Product ◽

Structural Revision ◽

Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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Synthetic studies towards the antiviral pyrazine derivative T-705

10.3390/ecsoc-13-00223 ◽

2009 ◽

Author(s):

Ulrich Jordis ◽

Sagar Beldar

Keyword(s):

Pyrazine Derivative ◽

Synthetic Studies

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Synthetic studies on the preparation of dinucleoside phenylphosphonates and phenylphosphonothioates via palladium(0) catalysed cross-coupling

Collection Symposium Series ◽

10.1135/css200507195 ◽

2005 ◽

Cited By ~ 4

Author(s):

Gaston Lavén ◽

Jacek Stawinski

Keyword(s):

Cross Coupling ◽

Synthetic Studies

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Synthetic studies on the P–C bond formation via a palladium-catalyzed cross-coupling reaction. Application to the synthesis of P-arylated nucleic acids

Collection Symposium Series ◽

10.1135/css200810214 ◽

2008 ◽

Cited By ~ 3

Author(s):

Marcin Kalek ◽

Jacek Stawinski

Keyword(s):

Nucleic Acids ◽

Bond Formation ◽

Coupling Reaction ◽

Cross Coupling ◽

Cross Coupling Reaction ◽

Palladium Catalyzed ◽

Synthetic Studies

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ChemInform Abstract: SYNTHETIC STUDIES IN THE ALKALOID FIELD PART 2, ON THE PREPARATION OF N-(BETA-INDOLYLETHYL)-DIHYDRO- AND N-(BETA-INDOLYLETHYL)-TETRAHYDROPYRIDINES BY CATALYTIC HYDROGENATION, AND THEIR ACID-INDUCED CYCLIZATION

Chemischer Informationsdienst ◽

10.1002/chin.197549297 ◽

1975 ◽

Vol 6 (49) ◽

pp. no-no

Author(s):

MAURI LOUNASMAA ◽

CARL-JOHAN JOHANSSON

Keyword(s):

Catalytic Hydrogenation ◽

Synthetic Studies

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ChemInform Abstract: SYNTHETIC STUDIES ON OPTICALLY ACTIVE β-LACTAMS. CHIRAL SYNTHESIS OF CARBAPENAM RING SYSTEM STARTING FROM L-ASPARTIC ACID

Chemischer Informationsdienst ◽

10.1002/chin.198101209 ◽

1981 ◽

Vol 12 (1) ◽

Author(s):

N. IKOTA ◽

H. SHIBATA ◽

K. KOGA

Keyword(s):

Aspartic Acid ◽

Ring System ◽

Optically Active ◽

Chiral Synthesis ◽

Synthetic Studies

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ChemInform Abstract: SYNTHETIC STUDIES ON OPTICALLY ACTIVE EPOXYTERPENES FROM L-GLUTAMIC ACID. II. YNTHESES OF R-(+)-10,11-EPOXYFARNESOL, R-(+)-, AND S-(-)-SQUALENE-2,3-OXIDE

Chemischer Informationsdienst ◽

10.1002/chin.197642363 ◽

1976 ◽

Vol 7 (42) ◽

pp. no-no

Author(s):

S. YAMADA ◽

N. OH-HASHI ◽

K. ACHIWA

Keyword(s):

Glutamic Acid ◽

Optically Active ◽

Synthetic Studies

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