Camphor-Based Chiral Auxiliary: Formal Synthesis of Enantiomerically Enriched b-Aminophosphonic Acids via PTC-Alkylation

G. CRAVOTTO; Giovanni Battista GIOVENZANA; R. PAGLIARIN; G. PALMISANO; M. SISTI

doi:10.1081/SCC-100103530

Camphor-Based Chiral Auxiliary: Formal Synthesis of Enantiomerically Enriched b-Aminophosphonic Acids via PTC-Alkylation

G. CRAVOTTO
, Giovanni Battista GIOVENZANA
, R. PAGLIARIN
, G. PALMISANO
, M. SISTI

Department of Pharmaceutical Sciences

Research output: Contribution to journal › Article › peer-review

Abstract

PTC-alkylation of a chiral non-racemic cyanomethyl phosphonic acid equivalent embodying the camphor skeleton gave rise to a formal entry into enantiomerically enriched b-amino-a-substituted phosphonic acids.

Original language	English
Pages (from-to)	1013-1020
Number of pages	8
Journal	Synthetic Communications
Volume	31
Issue number	7
DOIs	https://doi.org/10.1081/SCC-100103530
Publication status	Published - 2001

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10.1081/SCC-100103530

http://hdl.handle.net/11579/7293

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@article{46a45f93f99c47b4b205762030d96ffb,

title = "Camphor-Based Chiral Auxiliary: Formal Synthesis of Enantiomerically Enriched b-Aminophosphonic Acids via PTC-Alkylation",

abstract = "PTC-alkylation of a chiral non-racemic cyanomethyl phosphonic acid equivalent embodying the camphor skeleton gave rise to a formal entry into enantiomerically enriched b-amino-a-substituted phosphonic acids.",

author = "G. CRAVOTTO and GIOVENZANA, \{Giovanni Battista\} and R. PAGLIARIN and G. PALMISANO and M. SISTI",

note = "Funding Information: Financial support was provided by MURST and CNR.",

year = "2001",

doi = "10.1081/SCC-100103530",

language = "English",

volume = "31",

pages = "1013--1020",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor and Francis Ltd.",

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T1 - Camphor-Based Chiral Auxiliary: Formal Synthesis of Enantiomerically Enriched b-Aminophosphonic Acids via PTC-Alkylation

AU - CRAVOTTO, G.

AU - GIOVENZANA, Giovanni Battista

AU - PAGLIARIN, R.

AU - PALMISANO, G.

AU - SISTI, M.

N1 - Funding Information: Financial support was provided by MURST and CNR.

PY - 2001

Y1 - 2001

N2 - PTC-alkylation of a chiral non-racemic cyanomethyl phosphonic acid equivalent embodying the camphor skeleton gave rise to a formal entry into enantiomerically enriched b-amino-a-substituted phosphonic acids.

AB - PTC-alkylation of a chiral non-racemic cyanomethyl phosphonic acid equivalent embodying the camphor skeleton gave rise to a formal entry into enantiomerically enriched b-amino-a-substituted phosphonic acids.

UR - https://iris.uniupo.it/handle/11579/7293

U2 - 10.1081/SCC-100103530

DO - 10.1081/SCC-100103530

M3 - Article

SN - 0039-7911

VL - 31

SP - 1013

EP - 1020

JO - Synthetic Communications

JF - Synthetic Communications

IS - 7

ER -

Camphor-Based Chiral Auxiliary: Formal Synthesis of Enantiomerically Enriched b-Aminophosphonic Acids via PTC-Alkylation

Abstract

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