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Synlett 2006(19): 3366-3367  
DOI: 10.1055/s-2006-956459
SPOTLIGHT
© Georg Thieme Verlag Stuttgart · New York

BINOL: A Versatile Chiral Reagent

Satyendra Kumar Pandey*
Division of Organic Chemistry: Technology, National Chemical Laboratory, Pune 411008, India
e-Mail: s.pandey@ncl.res.in;

Dedicated to my research supervisor Dr. Pradeep Kumar


Further Information

Publication History

Publication Date:
23 November 2006 (online)

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Biographical Sketches

Satyendra Kumar Pandey was born in Kushinagar, U. P., India. He received his M.Sc. (Organic Chemistry) degree from D. D. U. ­Gorakhpur University, U. P. and M.E. degree from University of Delhi, India. He received a research fellowship after passing the CSIR-JRF National Eligibility Test (NET) and joined the research group of Dr. Pradeep Kumar at the National Chemical Laboratory, Pune, India. His main interests lie in the field of asymmetric syn­thesis of bioactive natural products and organic transformations.

Introduction

The aim of enantioselective synthesis or catalysis is to produce chiral products starting from achiral substrates by exploiting the presence of chiral reagents. The enantiomeric atropisomers of 1,1′-binaphthyl-2,2′-diol (BINOL) are the best-known representatives of axially chiral molecules and were first prepared as racemate in 1873 by von Richter. [1] BINOL is used for both stoichiometric and ­catalytic asymmetric reactions. [2] The chiral atropisomers (R)-1 ([α]20 D +35.5 THF, c 1), mp 205-211 °C and (S)-1 ([α]20 D -34.5, THF, c 1), mp 205-211 °C are stable at high temperature and allow numerous asymmetric reactions under various experimental conditions (Figure 1). [3] BINOL-mediated asymmetric oxidation, reduction and C-C bond-forming reactions are well-established reactions in ­organic synthesis. BINOL (1) can be easily prepared from 2-naphthol using Cu-amine complexes to give racemic BINOL which can be converted into (R)-BINOL [(R)-1] or (S)-BINOL [(S)-1] by enzymatic resolution [4] or via chemical resolution (Scheme 1). [5]

Figure 1

Scheme 1

Abstracts

(A) The catalytic asymmetric reduction of different ketones with transient hypervalent trialkoxy silanes in the presence of a small amount of a chiral nucleophile such as BINOL (1) underwent ­addition to the carbonyl group, forming the corresponding silyl-protected alcohols, which were cleaved during the work-up to give enantiomerically enriched alcohols. [6]

(B) Hosomi et al. reported an optically active lithium alkoxide which catalysed asymmetric reduction of imines with trimethoxy­silanes affording the expected amines in moderate ee (up to 72%). [7]

(C) Shibasaki et al. used lanthanum- or ytterbium-modified BINOL derivatives as catalysts in the asymmetric epoxidation of enones with tert-butyl hydroperoxide (TBHP). [8]

(D) Yamamoto et al. reported the first successful example of ­asymmetric induction which deals with a cyclisation in the ­presence of a BINOL-Al catalyst. Indeed, a catalyst prepared in situ from dimethyl zinc and optically pure (R)-(-)-BINOL pro­moted the cyclisation of 3-methylcitronellal to methylisopulegol as a single isomer with 90% ee. [9]

(E) Olsson et al. reported the Diels-Alder reaction between ‘noncompatible’ dienes and dienophiles by means of a temporary Al or Zr tethering. [10]

(F) Very recently, Pu, Yu and coworkers reported the highly enantioselective reaction of an alkynoate with aromatic and α,β-unsaturated aldehydes for the synthesis of optically active γ-hydroxy-α,β-acetylenic esters containing three adjacent and structurally very different functional groups which are very useful in the ­synthesis of highly functionalized organic molecules. [11]

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Figure 1

Scheme 1