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Control of diastereoselectivity by solvent effects in the addition of Grignard reagents to enantiopure t-butylsulfinimine: syntheses of the stereoisomers of the hydroxyl derivatives of sibutramine.
Org Lett. 2005 Jun 23;7(13):2599-602. doi: 10.1021/ol0507017.
Org Lett. 2005.
PMID: 15957900
First application of tunable alkyl or aryl sulfinamides to the stereoselective synthesis of a chiral amine: asymmetric synthesis of (R)-didesmethylsibutramine ((R)-DDMS) using (R)-triethylmethylsulfinamide ((R)-TESA).
Han Z, Krishnamurthy D, Pflum D, Grover P, Wald SA, Senanayake CH.
Han Z, et al. Among authors: wald sa.
Org Lett. 2002 Nov 14;4(23):4025-8. doi: 10.1021/ol026699q.
Org Lett. 2002.
PMID: 12423077
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New general sulfinylating process for asymmetric synthesis of enantiopure sulfinates and sulfoxides.
Lu BZ, Jin F, Zhang Y, Wu X, Wald SA, Senanayake CH.
Lu BZ, et al. Among authors: wald sa.
Org Lett. 2005 Apr 14;7(8):1465-8. doi: 10.1021/ol0501020.
Org Lett. 2005.
PMID: 15816728
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A new lithium alkoxide accelerated diastereoselective cyanation of ketones.
Wilkinson HS, Grover PT, Vandenbossche CP, Bakale RP, Bhongle NN, Wald SA, Senanayake CH.
Wilkinson HS, et al. Among authors: wald sa.
Org Lett. 2001 Feb 22;3(4):553-6. doi: 10.1021/ol0069608.
Org Lett. 2001.
PMID: 11178823
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Chiral mandelic acid template provides a highly practical solution for (S)-oxybutynin synthesis.
Grover PT, Bhongle NN, Wald SA, Senanayake CH.
Grover PT, et al. Among authors: wald sa.
J Org Chem. 2000 Sep 22;65(19):6283-7. doi: 10.1021/jo005562f.
J Org Chem. 2000.
PMID: 10987980
No abstract available.
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Albuterol. A pharmaceutical chemistry review of R-, S-, and RS-albuterol.
Bakale RP, Wald SA, Butler HT, Gao Y, Hong Y, Nie X, Zepp CM.
Bakale RP, et al. Among authors: wald sa.
Clin Rev Allergy Immunol. 1996 Spring;14(1):7-35. doi: 10.1007/BF02772200.
Clin Rev Allergy Immunol. 1996.
PMID: 8866169
Review.
No abstract available.
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