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38114-29-3

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38114-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38114-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,1 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38114-29:
(7*3)+(6*8)+(5*1)+(4*1)+(3*4)+(2*2)+(1*9)=103
103 % 10 = 3
So 38114-29-3 is a valid CAS Registry Number.

38114-29-3Relevant articles and documents

GLP-1 RECEPTOR MODULATORS

-

, (2016/06/28)

Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where "^^^^" represents either or both the R and S form of the compound) (I) where A, B, C, Y1, Y2, Z, R1, R2, R3, R4, R5, W1, n, p and q are as defined herein.

Asymmetric synthesis of 2,4,5-trisubstituted Δ2- thiazolines

Bengtsson, Christoffer,Nelander, Hanna,Almqvist, Fredrik

, p. 9916 - 9922 (2013/08/23)

Δ2-Thiazolines are interesting heterocycles that display a wide variety of biological characteristics. They are also common in chiral ligands used for asymmetric syntheses and as synthetic intermediates. Herein, we present asymmetric routes to

Addition of azomethine ylides to aldehydes: Mechanistic dichotomy of differentially substituted α-imino esters

Seashore-Ludlow, Brinton,Torssell, Staffan,Somfai, Peter

scheme or table, p. 3927 - 3933 (2010/09/18)

The formal 1,3-dipolar cycloaddition of azomethine ylides and aldehydes is explored, as hydrolysis of the resulting oxazolidine product gives facile access to valuable syn-β-arylβ-hydroxy-α-amino esters. The use of using benzaldehydederived imines as the ylide precursor results in 1,3-dipolar cycloaddition with high conversions but low diastereoselec-tivity. In contrast, the employment of benzophenone-derived imines as the ylide precursor results in an aldol reaction, which gives the intermediate oxazolidine in high diastereoselectivity and requires a weak acid catalyst to achieve higher conversions.

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