Olefinic-lactone cyclizations to macrocycles. - Wikidata - awgldk - TriplyDB

Olefinic-lactone cyclizations to macrocycles.

Olefinic-lactone cyclizations to macrocycles.

http://www.wikidata.org/entity/Q37396316

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Selected synthetic strategies to cyclophanes Olefinic-amide and olefinic-lactam cyclizations.Synthetic efforts towards the stereoselective synthesis of NF00659B1.Fluorinated Musk Fragrances: The CF2 Group as a Conformational Bias Influencing the Odour of Civetone and (R)-Muscone.

P2860

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P2860

Olefinic-lactone cyclizations to macrocycles.

http://www.wikidata.org/entity/Q37396316

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on January 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Olefinic-lactone cyclizations to macrocycles.

@en

Olefinic-lactone cyclizations to macrocycles.

@nl

type

label

Olefinic-lactone cyclizations to macrocycles.

@en

Olefinic-lactone cyclizations to macrocycles.

@nl

prefLabel

Olefinic-lactone cyclizations to macrocycles.

@en

Olefinic-lactone cyclizations to macrocycles.

@nl

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P1433

Organic Letters

P1476

Olefinic-lactone cyclizations to macrocycles.

@en

P2093

John C Rohanna

http://www.w3.org/2001/XMLSchema#string

Jon D Rainier

http://www.w3.org/2001/XMLSchema#string

P2860

Synthetic analogues of migrastatin that inhibit mammary tumor metastasis in mice

Macrocyclization by Ring-Closing Metathesis in the Total Synthesis of Natural Products: Reaction Conditions and Limitations

Total synthesis of the Hsp90 inhibitor geldanamycin.

The total synthesis of gambierol.

Recent methods for the synthesis of (E)-alkene units in macrocyclic natural products.

Macrolactonizations in the total synthesis of natural products.

A three-carbon (n+1+2) ring expansion method for the synthesis of macrocyclic enones. Application to muscone synthesis.

Total synthesis of thiopeptide antibiotics GE2270A, GE2270T, and GE2270C1.

Enantioselective Intramolecular Aldol Addition/Dehydration Reaction of a Macrocyclic Diketone: Synthesis of the Musk Odorants (R)-Muscone and (R,Z)-5-Muscenone

P304

493-495

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scholarly article

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10.1021/OL802737H

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P407

P433

2

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11

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2009-01-01T00:00:00Z

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23653605

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19072700

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2765781

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