Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver

Giovanni Casiraghi; Franca Zanardi; Giovanni Appendino; Gloria Rassu

doi:10.1021/cr990247i

Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver

Giovanni Casiraghi
, Franca Zanardi
, Giovanni Appendino
, Gloria Rassu

Risultato della ricerca: Contributo su rivista › Articolo in rivista › peer review

Abstract

The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.

Lingua originale	Inglese
pagine (da-a)	1929-1972
Numero di pagine	44
Rivista	Chemical Reviews
Volume	100
Numero di pubblicazione	6
DOI	https://doi.org/10.1021/cr990247i
Stato di pubblicazione	Pubblicato - giu 2000
Pubblicato esternamente	Sì

Accesso al documento

10.1021/cr990247i

Altri file e collegamenti

Link to publication in Scopus

Cita questo

@article{d0ecf103d4f2484cb2de64c18118ff55,

title = "Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver",

abstract = "The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.",

author = "Giovanni Casiraghi and Franca Zanardi and Giovanni Appendino and Gloria Rassu",

year = "2000",

month = jun,

doi = "10.1021/cr990247i",

language = "English",

volume = "100",

pages = "1929--1972",

journal = "Chemical Reviews",

issn = "0009-2665",

publisher = "American Chemical Society",

number = "6",

}

TY - JOUR

T1 - Vinylogous aldol reaction

T2 - a valuable, yet understated carbon-carbon bond-forming maneuver

AU - Casiraghi, Giovanni

AU - Zanardi, Franca

AU - Appendino, Giovanni

AU - Rassu, Gloria

PY - 2000/6

Y1 - 2000/6

N2 - The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.

AB - The vinylogous aldol reactions provides access to a range of structurally diverse targets but has long remained a marginally explored area of organic synthesis. However, its applications have burgeoned in the past few years. Examples are given to demonstrate that vinylogous dienolates and their synthons have a sumptuos aldol chemistry.

UR - https://www.scopus.com/pages/publications/0033690703

U2 - 10.1021/cr990247i

DO - 10.1021/cr990247i

M3 - Article

SN - 0009-2665

VL - 100

SP - 1929

EP - 1972

JO - Chemical Reviews

JF - Chemical Reviews

IS - 6

ER -

Vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver

Abstract

Accesso al documento

Altri file e collegamenti

Fingerprint

Cita questo