Pyrrolizidine alkaloids. A concise entry to (-)-pyrrolam A

Giovanni B. Giovenzana; Massimo Sisti; Giovanni Palmisano

doi:10.1016/S0957-4166(97)00010-4

Pyrrolizidine alkaloids. A concise entry to (-)-pyrrolam A

Giovanni B. Giovenzana
, Massimo Sisti
, Giovanni Palmisano

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

Abstract

The synthesis of (-)-pyrrolam A starting from (R)-prolinol is described. The key step is the dehydrative alkylation of a conveniently protected (R)-prolinol with triethyl methanetricarboxylae under the conditions of the mitsunobu reaction.

Lingua originale	Inglese
pagine (da-a)	515-518
Numero di pagine	4
Rivista	Tetrahedron Asymmetry
Volume	8
Numero di pubblicazione	4
DOI	https://doi.org/10.1016/S0957-4166(97)00010-4
Stato di pubblicazione	Pubblicato - 20 feb 1997
Pubblicato esternamente	Sì

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title = "Pyrrolizidine alkaloids. A concise entry to (-)-pyrrolam A",

abstract = "The synthesis of (-)-pyrrolam A starting from (R)-prolinol is described. The key step is the dehydrative alkylation of a conveniently protected (R)-prolinol with triethyl methanetricarboxylae under the conditions of the mitsunobu reaction.",

author = "Giovenzana, \{Giovanni B.\} and Massimo Sisti and Giovanni Palmisano",

note = "Funding Information: Acknowledgements Financial support at this work by the MURST (60\%) is gratefully acknowledged.",

year = "1997",

month = feb,

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doi = "10.1016/S0957-4166(97)00010-4",

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volume = "8",

pages = "515--518",

journal = "Tetrahedron Asymmetry",

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T1 - Pyrrolizidine alkaloids. A concise entry to (-)-pyrrolam A

AU - Giovenzana, Giovanni B.

AU - Sisti, Massimo

AU - Palmisano, Giovanni

N1 - Funding Information: Acknowledgements Financial support at this work by the MURST (60%) is gratefully acknowledged.

PY - 1997/2/20

Y1 - 1997/2/20

N2 - The synthesis of (-)-pyrrolam A starting from (R)-prolinol is described. The key step is the dehydrative alkylation of a conveniently protected (R)-prolinol with triethyl methanetricarboxylae under the conditions of the mitsunobu reaction.

AB - The synthesis of (-)-pyrrolam A starting from (R)-prolinol is described. The key step is the dehydrative alkylation of a conveniently protected (R)-prolinol with triethyl methanetricarboxylae under the conditions of the mitsunobu reaction.

UR - https://www.scopus.com/pages/publications/0031579466

U2 - 10.1016/S0957-4166(97)00010-4

DO - 10.1016/S0957-4166(97)00010-4

M3 - Article

SN - 0957-4166

VL - 8

SP - 515

EP - 518

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 4

ER -

Pyrrolizidine alkaloids. A concise entry to (-)-pyrrolam A

Abstract

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