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ethyl N-benzenesulfonylacetimidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

808755-55-7

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808755-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 808755-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,8,7,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 808755-55:
(8*8)+(7*0)+(6*8)+(5*7)+(4*5)+(3*5)+(2*5)+(1*5)=197
197 % 10 = 7
So 808755-55-7 is a valid CAS Registry Number.

808755-55-7Downstream Products

808755-55-7Relevant academic research and scientific papers

Three-component reactions of sulfonylimidates, silyl glyoxylates and N - Tert -butanesulfinyl aldimines: An efficient, diastereoselective, and enantioselective synthesis of cyclic N -sulfonylamidines

Yao, Ming,Lu, Chong-Dao

supporting information; experimental part, p. 2782 - 2785 (2011/07/07)

Three-component coupling reactions of sulfonylimidates, silyl glyoxylates and N-tert-butanesulfinyl aldimines efficiently provide cyclic N-sulfonylamidines containing free endocyclic N-H. The formation of two C-C bonds (contiguous stereogenic carbons), on

Catalytic Mannich-type reactions of Sulfonylimidates

Matsubara, Ryosuke,Berthiol, Florian,Nguyen, Huy V.,Kobayashi, Shu

experimental part, p. 1083 - 1102 (2009/12/25)

A novel nucleophile, sulfonylimidate, has been successfully employed in Mannich-type reactions. Due to electronwithdrawing property of sulfonyl group of sulfonylimidate, the acidity of α-proton is enhanced so that sulfonylimidate bearing no activating functional group at α-position is deprotonated by relatively weak base. DBU-catalyzed reactions of sulfonylimidates with protected imines in DMF provided the adducts in high yields with high anti selectivity. This reaction represents a wide substrate scope and a high catalytic turnover. A thorough kinetic study revealed that ratedetermining step is most likely deprotonation step in case of Ts-imidate. Alkali earth metal alkoxide and its HMDS salt also catalyze Mannich-type reactions of sulfonylimidates. The reactions catalyzed by Mg(O tBu)2 in DMF provided the adducts with high anti selectivity, while those catalyzed by [Sr(HMDS)2]2 gave syn selectivity. The asymmetric variant of Mannich-type reaction of sulfonylimidate was also achieved. Several transformations of sulfonylimidates to other functional groups were also demonstrated. Finally, direct-type catalytic formation of cβ-amino acid ester from aldehyde and sulfonylimidate was achieved via in situ formation of sulfonylimine and DBU-assisted hydrolysis of sulfonylimidate.

DBU-catalyzed addition reactions of sulfonylimidates

Matsubara, Ryosuke,Kobayashi, Shu

experimental part, p. 3009 - 3011 (2009/04/10)

Sulfonylimidates react with various types of N-protected imines in the presence of a catalytic amount of DBU to afford β-aminosulfonylimidates in high yields and high anti-selectivities. The experimental procedure is described in detail. Georg Thieme Verlag Stuttgart.

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