Synlett 2015; 26(05): 707-708
DOI: 10.1055/s-0034-1380270
spotlight
© Georg Thieme Verlag Stuttgart · New York

l-Proline and d-Proline (Chiral Amino Acid Catalysts)

Dhanaraju Mandalapu
Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow 226031, India   Email: dhanachems.18@gmail.com
› Author Affiliations
Further Information

Publication History

Publication Date:
19 February 2015 (eFirst)

Introduction

l-Proline and d-proline are often used as asymmetric organocatalysts for a variety of organic reactions, due to their conformational rigidity as compared to other amino acids. Where l-proline is a natural non-essential amino ­acid, d-proline is an unnatural amino acid, with one basic and one acidic center each. Owing to their wide applicability in asymmetric organocatalysis for the synthesis of enantiopure compounds in the last decade, this article is an update to spotlight No. 60 and 168.[1]

Zoom Image
Figure 1 General structures of l-proline and d-proline

In the 21st century, the use of small organic molecules as chiral organocatalysts has become a powerful strategy and an attractive field in organic chemistry.[2] Among the catalysts developed, l/d-proline and its derivatives catalyzed a wide range of reactions.[3] l/d-Proline collectively has the application as catalysts in asymmetric Mannich reactions for chiral β-aminocarbonyls,[4] aldehyde aldol reaction for the synthesis of erythrose equivalents,[5] domino Mannich–Aza-Michael reactions,[6] Morita–Bayllis–Hillman reactions,[7] Heck cross-coupling reactions,[8] multicomponent reations,[9] in the synthesis of bioactive diketopiperazines,[10] spirooxindazoles[11] and also in phosphodiester bond linkages to recognize DNA and RNAs[12] and in bifunctional catalysts, it acts as co-catalyst.[13] In addition, the application in the preparation of a wide variety of chiral catalysts like chiral MOFs,[14] Barbas–List aldol catalysts,[15] bile acid catalysts[16] and has excellent use in autocatalysis strategy, to form the initial enantiorich isomers, which further autocatalyze the reactions.[17] l/d-proline also served as building blocks in construction of chiral 3D architectures.[18]

Table 1 Use of L-Proline and d-Proline (Chiral Amino Acid Catalysts)

(A) In a recent one-pot chiral synthesis, the Shi group[19] used l/d-proline as Lewis base, in the presence of a chiral auxiliary group to synthesize substituted isoxazoline-N-oxides highly chemo-/enantio­selectively in good yields. With either l- or d-proline, the absolute stereochemistry of isoxazolidines was identical.

(B) If an additive is used, l/d-proline catalyze the cross-aldol reaction of ethyl benzoyl(diethoxymethyl)phosphinate and acetone for the synthesis of α-hydroxy-H-phosphinate synthons in an organocatalyzed reaction.[20] These are used in the synthesis of a variety of organic phosphorus compounds.

(C) In an enantioselective asymmetric hetero-Diels–Alder reaction of enones and aldehydes, the Zhao group[21] used supramolecular bifunctional organocatalysts, which were synthesized by using l/d-proline and Cinchona alkaloids (quinidine thiourea), linked to each other through ionic hydrogen bonds for high stereoselectivity.

(D) l/d-Proline catalyze the asymmetric Morita–Baylis–Hillman (MBH) reaction in the presence of brucine-N-oxide as co-catalyst, through iminium intermediates.[7] This dual catalytic system forms MBH products with opposite configuration with the respective l/d-proline in good enantioselectivities.

(E) Rawat et al.[22] developed a novel l/d-proline catalyzed sequential α-amination–reductive cyclization of o-nitrohydroxy cinnamaldehydes for the construction of 3-substituted chiral tetrahydroquinolines (THQ) with good enantioselectivity, which were further applied in the total synthesis of bioactive (−)-sumanirole (96% ee) and (S)-903 (92% ee).

 
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