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781658-08-0

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781658-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 781658-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,1,6,5 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 781658-08:
(8*7)+(7*8)+(6*1)+(5*6)+(4*5)+(3*8)+(2*0)+(1*8)=200
200 % 10 = 0
So 781658-08-0 is a valid CAS Registry Number.

781658-08-0Downstream Products

781658-08-0Relevant academic research and scientific papers

Base-promoted addition of DMA with 1,1-diarylethylenes: Application to a total synthesis of (-)-sacidumlignan B

Luo, Zhen-Biao,Peng, Yu,Wang, Ya-Wen

supporting information, p. 2054 - 2057 (2020/03/27)

A base-promoted addition of DMA (N,N-dimethylacetamide) to 1,1-diarylethylenes has been developed, and it provides a new strategy for the synthesis of N,N-dimethyl-4,4-diarylbutanamides from 1,1-diarylethylenes at room temperature. This method allows us to achieve the goal of synthesizing (-)-sacidumlignan B, and provides simple operation and broad substrate scope by avoiding the use of transition metal catalysts.

Triflimide-catalyzed allylsilane annulations of benzylic alcohols for the divergent synthesis of indanes and tetralins

Reddel, Jordan C. T.,Wang, Weiwei,Koukounas, Kalli,Thomson, Regan J.

, p. 2156 - 2160 (2017/03/09)

The development of a triflimide-catalyzed annulation of benzylic alcohols with allylsilanes for the synthesis of indane or tetralin structures is reported. In this fragment coupling reaction, complexity is built rapidly from readily available starting materials to yield diverse sets of products with up to three contiguous stereocenters. Indanes or tetralins can be generated from common precursors depending on the structure of the allylsilane reagent used. The concise synthesis of several lignan natural products highlights the utility of this newly devised methodology.

Total synthesis of (-)-sacidumlignans B and D

Rout, Jeetendra Kumar,Ramana

experimental part, p. 1566 - 1571 (2012/04/04)

The first total synthesis of naturally occurring sacidumlignans A (1), B (2), and D (4) was executed and the absolute configuration of 2 and 4 was determined. A diastereoselective α- methylation of a lactone was used as the key step for the control of the chiral centers of the central lignan core. An acid mediated dehydrative cyclization of an aldehyde to construct the dihydronaphthalene unit of 2 and the aromatization of the intermediate dihydronaphthalene derivative to synthesize 1 are the key reactions employed in this regard.

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