ChemInform Abstract: Total Synthesis of C31-Methyl Ketone Apocarotenoids. Part 3. Structure of Hopkinsiaxanthin: First Total Synthesis of (all-E)-(3S)- and (9Z)-(3S)-7′-Apohopkinsiaxanthin.

ChemInform ◽  
2010 ◽  
Vol 29 (11) ◽  
pp. no-no
Author(s):  
J. A. HAUGAN ◽  
E. LOBKOVSKY ◽  
S. LIAAEN-JENSEN
Keyword(s):  
Total Synthesis ◽  
Methyl Ketone

A total synthesis of magallanesine: DMF acetal mediated cyclodehydration of a methyl ketone thioimide

1989 ◽  
Vol 30 (21) ◽  
pp. 2743-2746 ◽  
Author(s):  
Francis G. Fang ◽  
Gregg B. Feigelson ◽  
Samuel J. Danishefsky
Keyword(s):  
Total Synthesis ◽  
Methyl Ketone

VALERIAN ALKALOIDS: FIRST TOTAL SYNTHESIS OF A NAPHTHYRIDYL METHYL KETONE

2000 ◽  
Vol 6 (1) ◽  
Author(s):  
Eugen Barbu ◽  
Jens J. Wolff ◽  
Ion Bolocan ◽  
Flavian Cuiban
Keyword(s):  
Total Synthesis ◽  
Methyl Ketone

scholarly journals Total Synthesis of C31-Methyl Ketone Apocarotenoids 2: The First Total Synthesis of (3R)-Triophaxanthin.

1997 ◽  
Vol 51 ◽  
pp. 1096-1103 ◽  
Author(s):  
Jarle André Haugan ◽  
Pål Songe ◽  
Christian Rømming ◽  
Frode Rise ◽  
Michael P. Hartshorn ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Methyl Ketone

scholarly journals Total Synthesis of C31-Methyl Ketone Apocarotenoids: Sintaxanthin and (3R)-3-Hydroxysintaxanthin.

1994 ◽  
Vol 48 ◽  
pp. 657-664 ◽  
Author(s):  
Jarle André Haugan ◽  
Per-Erik Jansson ◽  
Bengt Lindqvist ◽  
Graciela Andrei ◽  
Robert Snoeck ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Methyl Ketone

Unified Approach to ent-Eudesmane-type Terpenoid Synthesis: Total Synthesis of Sinupol and Eutyscoparin A

Synthesis ◽  
2021 ◽  
Author(s):  
Koichiro Ota ◽  
Kazuo Kamaike ◽  
Hiroaki Miyaoka
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Large Class ◽  
Methyl Ketone ◽  
Alder Reaction ◽  
Diels Alder ◽  
Synthetic Approach ◽  
Unified Approach ◽  
Diels Alder Reaction

ent-Eudesmane-type terpenoids constitute a large class of natural products derived from plants, animals, and bacteria. We describe a synthetic approach to two ent-eudesmane-type terpenoids, sinupol, and eutyscoparin A, that relies on a key π-facial- and endo/exo-selective intramolecular Diels–Alder reaction to set the C-5–C-10 stereotriads. Further key transformations of trans-fused decalin include conversion to methyl ketone via a versatile thioester intermediate and appropriate functionalization toward target compounds.

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